Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 16 700002 700002 + Silent SNP G G A TCGA-GV-A3JX-01A-11D-A20D-08 TCGA-GV-A3JX-10A-01D-A20D-08 g.chr16:700002G>A c.114G>A c.(112-114)ctG>ctA p.L38L BLCA 16 700265 700265 + Silent SNP C C T TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr16:700265C>T c.291C>T c.(289-291)gtC>gtT p.V97V BLCA 16 703599 703599 + Silent SNP G G A TCGA-BT-A0S7-01A-11D-A10S-08 TCGA-BT-A0S7-10A-01D-A10S-08 g.chr16:703599G>A c.1308G>A c.(1306-1308)cgG>cgA p.R436R BLCA 16 705107 705107 + Missense_Mutation SNP G G C TCGA-CF-A9FF-01A-11D-A38G-08 TCGA-CF-A9FF-10A-01D-A38J-08 g.chr16:705107G>C c.1516G>C c.(1516-1518)Gac>Cac p.D506H BLCA 16 708543 708543 + Missense_Mutation SNP G G A TCGA-G2-A2EC-01A-11D-A17V-08 TCGA-G2-A2EC-10A-01D-A17V-08 g.chr16:708543G>A c.2785G>A c.(2785-2787)Gag>Aag p.E929K BLCA 16 708562 708562 + Missense_Mutation SNP C C T TCGA-ZF-A9RE-01A-11D-A38G-08 TCGA-ZF-A9RE-10A-01D-A38J-08 g.chr16:708562C>T c.2804C>T c.(2803-2805)aCg>aTg p.T935M BLCA 16 708562 708562 + Missense_Mutation SNP C C T TCGA-ZF-AA52-01A-12D-A391-08 TCGA-ZF-AA52-10A-01D-A394-08 g.chr16:708562C>T c.2804C>T c.(2803-2805)aCg>aTg p.T935M BLCA 16 711673 711673 + Missense_Mutation SNP G G T TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr16:711673G>T c.3750G>T c.(3748-3750)gaG>gaT p.E1250D BLCA 16 711933 711933 + Missense_Mutation SNP C C A TCGA-FJ-A3Z9-01A-11D-A26M-08 TCGA-FJ-A3Z9-10A-01D-A26K-08 g.chr16:711933C>A c.3907C>A c.(3907-3909)Ctg>Atg p.L1303M BLCA 16 712823 712823 + Silent SNP C C T TCGA-HQ-A5NE-01A-12D-A289-08 TCGA-HQ-A5NE-10A-01D-A289-08 g.chr16:712823C>T c.4290C>T c.(4288-4290)ctC>ctT p.L1430L BLCA 16 715958 715958 + Silent SNP C C G TCGA-HQ-A5NE-01A-12D-A289-08 TCGA-HQ-A5NE-10A-01D-A289-08 g.chr16:715958C>G c.4443C>G c.(4441-4443)ctC>ctG p.L1481L BLCA 16 716290 716290 + Silent SNP C C T TCGA-DK-A3IN-01A-11D-A20D-08 TCGA-DK-A3IN-10A-01D-A20D-08 g.chr16:716290C>T c.4680C>T c.(4678-4680)ttC>ttT p.F1560F BLCA 16 716521 716521 + Missense_Mutation SNP G G A TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr16:716521G>A c.4807G>A c.(4807-4809)Gtc>Atc p.V1603I BLCA 16 716521 716521 + Missense_Mutation SNP G G T TCGA-DK-A3IK-01A-32D-A21A-08 TCGA-DK-A3IK-10A-01D-A21A-08 g.chr16:716521G>T c.4807G>T c.(4807-4809)Gtc>Ttc p.V1603F BLCA 16 716773 716773 + Missense_Mutation SNP A A G TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr16:716773A>G c.4985A>G c.(4984-4986)tAc>tGc p.Y1662C BRCA 16 701847 701847 + Silent SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr16:701847A>C c.861A>C c.(859-861)gcA>gcC p.A287A BRCA 16 705776 705776 + Missense_Mutation SNP C C T TCGA-AO-A1KR-01A-12D-A142-09 TCGA-AO-A1KR-10A-01D-A142-09 g.chr16:705776C>T c.1853C>T c.(1852-1854)cCc>cTc p.P618L BRCA 16 708527 708527 + Silent SNP G G A TCGA-E2-A155-01A-11D-A12B-09 TCGA-E2-A155-10A-01D-A12B-09 g.chr16:708527G>A c.2769G>A c.(2767-2769)ctG>ctA p.L923L BRCA 16 709364 709364 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr16:709364G>A c.3172G>A c.(3172-3174)Gaa>Aaa p.E1058K BRCA 16 711733 711733 + Silent SNP G G A TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr16:711733G>A c.3810G>A c.(3808-3810)caG>caA p.Q1270Q BRCA 16 715685 715685 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr16:715685G>A c.4318G>A c.(4318-4320)Gag>Aag p.E1440K CESC 16 705684 705684 + Silent SNP G G A TCGA-C5-A1BQ-01C-11D-A20U-09 TCGA-C5-A1BQ-10A-01D-A20U-09 g.chr16:705684G>A c.1830G>A c.(1828-1830)caG>caA p.Q610Q CESC 16 705701 705701 + Missense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr16:705701C>T c.1847C>T c.(1846-1848)tCa>tTa p.S616L CESC 16 707790 707790 + Silent SNP G G A TCGA-EA-A410-01A-11D-A243-09 TCGA-EA-A410-10A-01D-A243-09 g.chr16:707790G>A c.2502G>A c.(2500-2502)gcG>gcA p.A834A CESC 16 709007 709007 + Missense_Mutation SNP G G A TCGA-DS-A5RQ-01A-11D-A28B-09 TCGA-DS-A5RQ-10A-01D-A28E-09 g.chr16:709007G>A c.3007G>A c.(3007-3009)Gag>Aag p.E1003K CESC 16 711352 711352 + Missense_Mutation SNP C C G TCGA-EK-A3GM-01A-11D-A20U-09 TCGA-EK-A3GM-10A-01D-A20U-09 g.chr16:711352C>G c.3524C>G c.(3523-3525)tCt>tGt p.S1175C CESC 16 712707 712707 + Silent SNP C C T TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr16:712707C>T c.4174C>T c.(4174-4176)Ctg>Ttg p.L1392L CESC 16 717452 717452 + Missense_Mutation SNP G G A TCGA-EA-A3HR-01A-11D-A20U-09 TCGA-EA-A3HR-10A-01D-A20U-09 g.chr16:717452G>A c.5110G>A c.(5110-5112)Gac>Aac p.D1704N CHOL 16 703802 703802 + Splice_Site SNP C C T TCGA-ZH-A8Y6-01A-11D-A417-09 TCGA-ZH-A8Y6-10A-01D-A41A-09 g.chr16:703802C>T c.1436C>T c.(1435-1437)aCg>aTg p.T479M COAD 16 703387 703387 + Missense_Mutation SNP C C A TCGA-A6-3808-01A-01W-0995-10 TCGA-A6-3808-11A-01W-0995-10 g.chr16:703387C>A c.1169C>A c.(1168-1170)gCg>gAg p.A390E COAD 16 703647 703647 + Silent SNP A A G TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr16:703647A>G c.1356A>G c.(1354-1356)ccA>ccG p.P452P COAD 16 705118 705118 + Silent SNP C C A TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr16:705118C>A c.1527C>A c.(1525-1527)gcC>gcA p.A509A COAD 16 705360 705360 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr16:705360T>C c.1610T>C c.(1609-1611)gTg>gCg p.V537A COAD 16 706340 706340 + Missense_Mutation SNP G G T TCGA-D5-6922-01A-11D-1924-10 TCGA-D5-6922-10A-01D-1924-10 g.chr16:706340G>T c.2005G>T c.(2005-2007)Gat>Tat p.D669Y COAD 16 706404 706404 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr16:706404G>A c.2069G>A c.(2068-2070)cGg>cAg p.R690Q COAD 16 708330 708330 + Missense_Mutation SNP C C T TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr16:708330C>T c.2752C>T c.(2752-2754)Cgc>Tgc p.R918C COAD 16 709248 709248 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr16:709248C>T c.3056C>T c.(3055-3057)cCg>cTg p.P1019L COAD 16 710629 710629 + Silent SNP C C T TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr16:710629C>T c.3306C>T c.(3304-3306)ccC>ccT p.P1102P COAD 16 711354 711354 + Missense_Mutation SNP G G T TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr16:711354G>T c.3526G>T c.(3526-3528)Gcc>Tcc p.A1176S COAD 16 711950 711950 + Silent SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr16:711950C>T c.3924C>T c.(3922-3924)taC>taT p.Y1308Y COAD 16 712760 712760 + Silent SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:712760C>T c.4227C>T c.(4225-4227)gtC>gtT p.V1409V COAD 16 716059 716059 + Missense_Mutation SNP C C T TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr16:716059C>T c.4544C>T c.(4543-4545)aCg>aTg p.T1515M COAD 16 716916 716916 + Silent SNP G G A TCGA-AA-A02O-01A-21W-A096-10 TCGA-AA-A02O-11A-11W-A096-10 g.chr16:716916G>A c.5016G>A c.(5014-5016)aaG>aaA p.K1672K COAD 16 717523 717523 + Silent SNP G G T TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr16:717523G>T c.5181G>T c.(5179-5181)ccG>ccT p.P1727P COADREAD 16 703387 703387 + Missense_Mutation SNP C C A TCGA-A6-3808-01A-01W-0995-10 TCGA-A6-3808-11A-01W-0995-10 g.chr16:703387C>A c.1169C>A c.(1168-1170)gCg>gAg p.A390E COADREAD 16 703647 703647 + Silent SNP A A G TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr16:703647A>G c.1356A>G c.(1354-1356)ccA>ccG p.P452P COADREAD 16 705118 705118 + Silent SNP C C A TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr16:705118C>A c.1527C>A c.(1525-1527)gcC>gcA p.A509A COADREAD 16 705360 705360 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr16:705360T>C c.1610T>C c.(1609-1611)gTg>gCg p.V537A COADREAD 16 706340 706340 + Missense_Mutation SNP G G T TCGA-D5-6922-01A-11D-1924-10 TCGA-D5-6922-10A-01D-1924-10 g.chr16:706340G>T c.2005G>T c.(2005-2007)Gat>Tat p.D669Y COADREAD 16 706404 706404 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr16:706404G>A c.2069G>A c.(2068-2070)cGg>cAg p.R690Q COADREAD 16 708330 708330 + Missense_Mutation SNP C C T TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr16:708330C>T c.2752C>T c.(2752-2754)Cgc>Tgc p.R918C COADREAD 16 709248 709248 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr16:709248C>T c.3056C>T c.(3055-3057)cCg>cTg p.P1019L COADREAD 16 710629 710629 + Silent SNP C C T TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr16:710629C>T c.3306C>T c.(3304-3306)ccC>ccT p.P1102P COADREAD 16 711354 711354 + Missense_Mutation SNP G G T TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr16:711354G>T c.3526G>T c.(3526-3528)Gcc>Tcc p.A1176S COADREAD 16 711950 711950 + Silent SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr16:711950C>T c.3924C>T c.(3922-3924)taC>taT p.Y1308Y COADREAD 16 712760 712760 + Silent SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:712760C>T c.4227C>T c.(4225-4227)gtC>gtT p.V1409V COADREAD 16 716059 716059 + Missense_Mutation SNP C C T TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr16:716059C>T c.4544C>T c.(4543-4545)aCg>aTg p.T1515M COADREAD 16 716916 716916 + Silent SNP G G A TCGA-AA-A02O-01A-21W-A096-10 TCGA-AA-A02O-11A-11W-A096-10 g.chr16:716916G>A c.5016G>A c.(5014-5016)aaG>aaA p.K1672K COADREAD 16 717523 717523 + Silent SNP G G T TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr16:717523G>T c.5181G>T c.(5179-5181)ccG>ccT p.P1727P DLBC 16 703648 703648 + Missense_Mutation SNP A A G TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr16:703648A>G c.1357A>G c.(1357-1359)Atg>Gtg p.M453V DLBC 16 705344 705344 + Silent SNP C C A TCGA-GR-7351-01A-11D-2210-10 TCGA-GR-7351-10A-01D-2210-10 g.chr16:705344C>A c.1594C>A c.(1594-1596)Cgg>Agg p.R532R DLBC 16 708308 708308 + Silent SNP G G A TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr16:708308G>A c.2730G>A c.(2728-2730)gtG>gtA p.V910V DLBC 16 711429 711429 + Missense_Mutation SNP C C T TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chr16:711429C>T c.3601C>T c.(3601-3603)Ctc>Ttc p.L1201F DLBC 16 716494 716494 + Missense_Mutation SNP G G A TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr16:716494G>A c.4780G>A c.(4780-4782)Gct>Act p.A1594T DLBC 16 716971 716971 + Silent SNP C C T TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr16:716971C>T c.5071C>T c.(5071-5073)Ctg>Ttg p.L1691L ESCA 16 701947 701947 + Missense_Mutation SNP G G C TCGA-LN-A4MR-01A-11D-A28B-09 TCGA-LN-A4MR-10A-01D-A28E-09 g.chr16:701947G>C c.961G>C c.(961-963)Gag>Cag p.E321Q ESCA 16 708575 708575 + Silent SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr16:708575C>T c.2817C>T c.(2815-2817)gaC>gaT p.D939D ESCA 16 708985 708985 + Silent SNP C C A TCGA-JY-A6FG-01A-11D-A33E-09 TCGA-JY-A6FG-10A-01D-A33H-09 g.chr16:708985C>A c.2985C>A c.(2983-2985)ctC>ctA p.L995L ESCA 16 710154 710154 + Missense_Mutation SNP C C G TCGA-LN-A5U7-01A-11D-A31U-09 TCGA-LN-A5U7-10A-01D-A31U-09 g.chr16:710154C>G c.3281C>G c.(3280-3282)tCt>tGt p.S1094C ESCA 16 711660 711660 + Missense_Mutation SNP C C T TCGA-L5-A8NE-01A-11D-A37C-09 TCGA-L5-A8NE-11A-11D-A37F-09 g.chr16:711660C>T c.3737C>T c.(3736-3738)aCc>aTc p.T1246I ESCA 16 712011 712011 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr16:712011C>T c.3985C>T c.(3985-3987)Cgt>Tgt p.R1329C GBM 16 701986 701986 + Missense_Mutation SNP G G A TCGA-06-0157-01A-01D-1491-08 TCGA-06-0157-10A-01D-1491-08 g.chr16:701986G>A c.1000G>A c.(1000-1002)Gtg>Atg p.V334M GBM 16 703407 703407 + Missense_Mutation SNP G G A TCGA-06-5408-01A-01D-1696-08 TCGA-06-5408-10A-01D-1696-08 g.chr16:703407G>A c.1189G>A c.(1189-1191)Gtg>Atg p.V397M GBM 16 703568 703568 + Missense_Mutation SNP C C T TCGA-06-0158-01A-01D-1491-08 TCGA-06-0158-10A-01D-1491-08 g.chr16:703568C>T c.1277C>T c.(1276-1278)tCg>tTg p.S426L GBM 16 703624 703624 + Missense_Mutation SNP T T G TCGA-06-6701-01A-11D-1845-08 TCGA-06-6701-10A-01D-1845-08 g.chr16:703624T>G c.1333T>G c.(1333-1335)Tgc>Ggc p.C445G GBM 16 711897 711897 + Nonsense_Mutation SNP C C T TCGA-76-6283-01A-11D-1845-08 TCGA-76-6283-10A-01D-1845-08 g.chr16:711897C>T c.3871C>T c.(3871-3873)Cga>Tga p.R1291* GBM 16 715745 715745 + Missense_Mutation SNP C C T TCGA-06-2559-01A-01D-1494-08 TCGA-06-2559-10A-01D-1494-08 g.chr16:715745C>T c.4378C>T c.(4378-4380)Cgg>Tgg p.R1460W GBMLGG 16 701986 701986 + Missense_Mutation SNP G G A TCGA-06-0157-01A-01D-1491-08 TCGA-06-0157-10A-01D-1491-08 g.chr16:701986G>A c.1000G>A c.(1000-1002)Gtg>Atg p.V334M GBMLGG 16 703407 703407 + Missense_Mutation SNP G G A TCGA-06-5408-01A-01D-1696-08 TCGA-06-5408-10A-01D-1696-08 g.chr16:703407G>A c.1189G>A c.(1189-1191)Gtg>Atg p.V397M GBMLGG 16 703568 703568 + Missense_Mutation SNP C C T TCGA-06-0158-01A-01D-1491-08 TCGA-06-0158-10A-01D-1491-08 g.chr16:703568C>T c.1277C>T c.(1276-1278)tCg>tTg p.S426L GBMLGG 16 703624 703624 + Missense_Mutation SNP T T G TCGA-06-6701-01A-11D-1845-08 TCGA-06-6701-10A-01D-1845-08 g.chr16:703624T>G c.1333T>G c.(1333-1335)Tgc>Ggc p.C445G GBMLGG 16 705148 705148 + Splice_Site SNP G G A TCGA-QH-A86X-01A-11D-A36O-08 TCGA-QH-A86X-10A-01D-A367-08 g.chr16:705148G>A c.e14+1 GBMLGG 16 705313 705313 + Silent SNP G G A TCGA-E1-A7YM-01A-11D-A34A-08 TCGA-E1-A7YM-10A-01D-A34A-08 g.chr16:705313G>A c.1563G>A c.(1561-1563)gcG>gcA p.A521A GBMLGG 16 709106 709106 + Frame_Shift_Del DEL C C - TCGA-HT-8105-01A-11D-2395-08 TCGA-HT-8105-10A-01D-2396-08 g.chr16:709106delC c.3032delC c.(3031-3033)gccfs p.A1011fs GBMLGG 16 711897 711897 + Nonsense_Mutation SNP C C T TCGA-76-6283-01A-11D-1845-08 TCGA-76-6283-10A-01D-1845-08 g.chr16:711897C>T c.3871C>T c.(3871-3873)Cga>Tga p.R1291* GBMLGG 16 715745 715745 + Missense_Mutation SNP C C T TCGA-06-2559-01A-01D-1494-08 TCGA-06-2559-10A-01D-1494-08 g.chr16:715745C>T c.4378C>T c.(4378-4380)Cgg>Tgg p.R1460W GBMLGG 16 716482 716482 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:716482G>T c.4768G>T c.(4768-4770)Gac>Tac p.D1590Y HNSC 16 701826 701826 + Splice_Site SNP G G T TCGA-CV-7440-01A-11D-2129-08 TCGA-CV-7440-10A-01D-2129-08 g.chr16:701826G>T c.e9-1 HNSC 16 703414 703414 + Missense_Mutation SNP C C T TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr16:703414C>T c.1196C>T c.(1195-1197)aCg>aTg p.T399M HNSC 16 703573 703573 + Missense_Mutation SNP C C A TCGA-CV-7254-01A-11D-2012-08 TCGA-CV-7254-10A-01D-2013-08 g.chr16:703573C>A c.1282C>A c.(1282-1284)Cag>Aag p.Q428K HNSC 16 705335 705335 + Missense_Mutation SNP C C T TCGA-CR-6474-01A-11D-1870-08 TCGA-CR-6474-10A-01D-1870-08 g.chr16:705335C>T c.1585C>T c.(1585-1587)Cgg>Tgg p.R529W HNSC 16 706411 706411 + Nonsense_Mutation SNP C C G TCGA-BA-5152-01A-02D-1870-08 TCGA-BA-5152-10A-01D-1870-08 g.chr16:706411C>G c.2076C>G c.(2074-2076)taC>taG p.Y692* HNSC 16 708987 708987 + Missense_Mutation SNP G G T TCGA-BA-A6DA-01A-31D-A31L-08 TCGA-BA-A6DA-10A-01D-A31J-08 g.chr16:708987G>T c.2987G>T c.(2986-2988)tGg>tTg p.W996L HNSC 16 711364 711364 + Missense_Mutation SNP G G A TCGA-MT-A67D-01A-31D-A30E-08 TCGA-MT-A67D-10A-01D-A30H-08 g.chr16:711364G>A c.3536G>A c.(3535-3537)cGa>cAa p.R1179Q HNSC 16 711667 711667 + Silent SNP C C A TCGA-CV-A460-01A-21D-A25D-08 TCGA-CV-A460-10A-01D-A25E-08 g.chr16:711667C>A c.3744C>A c.(3742-3744)ctC>ctA p.L1248L HNSC 16 711778 711778 + Silent SNP C C T TCGA-BA-5558-01A-01D-1512-08 TCGA-BA-5558-10A-01D-1512-08 g.chr16:711778C>T c.3855C>T c.(3853-3855)atC>atT p.I1285I HNSC 16 712044 712044 + Missense_Mutation SNP G G A TCGA-CV-7099-01A-41D-2012-08 TCGA-CV-7099-10A-01D-2013-08 g.chr16:712044G>A c.4018G>A c.(4018-4020)Gat>Aat p.D1340N HNSC 16 715685 715685 + Missense_Mutation SNP G G A TCGA-CV-7429-01A-11D-2129-08 TCGA-CV-7429-10A-01D-2129-08 g.chr16:715685G>A c.4318G>A c.(4318-4320)Gag>Aag p.E1440K HNSC 16 715788 715788 + Missense_Mutation SNP A A G TCGA-CV-7254-01A-11D-2012-08 TCGA-CV-7254-10A-01D-2013-08 g.chr16:715788A>G c.4421A>G c.(4420-4422)cAg>cGg p.Q1474R HNSC 16 716348 716348 + Missense_Mutation SNP G G C TCGA-CQ-5326-01A-01D-1870-08 TCGA-CQ-5326-10A-01D-1870-08 g.chr16:716348G>C c.4738G>C c.(4738-4740)Gag>Cag p.E1580Q HNSC 16 716485 716485 + Silent SNP C C T TCGA-BA-5558-01A-01D-1512-08 TCGA-BA-5558-10A-01D-1512-08 g.chr16:716485C>T c.4771C>T c.(4771-4773)Cta>Tta p.L1591L HNSC 16 716533 716533 + Missense_Mutation SNP G G A TCGA-CV-A6JM-01A-11D-A31L-08 TCGA-CV-A6JM-10A-01D-A31J-08 g.chr16:716533G>A c.4819G>A c.(4819-4821)Gac>Aac p.D1607N HNSC 16 716723 716723 + Silent SNP G G A TCGA-MT-A67D-01A-31D-A30E-08 TCGA-MT-A67D-10A-01D-A30H-08 g.chr16:716723G>A c.4935G>A c.(4933-4935)ggG>ggA p.G1645G KICH 16 705360 705360 + Missense_Mutation SNP T T C TCGA-KO-8405-01A-11D-2310-10 TCGA-KO-8405-11A-01D-2311-10 g.chr16:705360T>C c.1610T>C c.(1609-1611)gTg>gCg p.V537A KIPAN 16 700677 700677 + Missense_Mutation SNP A A G TCGA-B4-5836-01A-11D-1669-08 TCGA-B4-5836-10A-01D-1669-08 g.chr16:700677A>G c.527A>G c.(526-528)aAc>aGc p.N176S KIPAN 16 703789 703789 + Missense_Mutation SNP C C G TCGA-2Z-A9J8-01A-11D-A42J-10 TCGA-2Z-A9J8-10A-01D-A42M-10 g.chr16:703789C>G c.1423C>G c.(1423-1425)Cac>Gac p.H475D KIPAN 16 705360 705360 + Missense_Mutation SNP T T C TCGA-KO-8405-01A-11D-2310-10 TCGA-KO-8405-11A-01D-2311-10 g.chr16:705360T>C c.1610T>C c.(1609-1611)gTg>gCg p.V537A KIPAN 16 707787 707787 + Silent SNP C C T TCGA-P4-A5E6-01A-11D-A28G-10 TCGA-P4-A5E6-11A-22D-A28G-10 g.chr16:707787C>T c.2499C>T c.(2497-2499)ccC>ccT p.P833P KIPAN 16 716291 716291 + Missense_Mutation SNP C C A TCGA-DW-7841-01A-11D-2136-08 TCGA-DW-7841-10A-01D-2136-08 g.chr16:716291C>A c.4681C>A c.(4681-4683)Cgt>Agt p.R1561S KIRC 16 700677 700677 + Missense_Mutation SNP A A G TCGA-B4-5836-01A-11D-1669-08 TCGA-B4-5836-10A-01D-1669-08 g.chr16:700677A>G c.527A>G c.(526-528)aAc>aGc p.N176S KIRP 16 703789 703789 + Missense_Mutation SNP C C G TCGA-2Z-A9J8-01A-11D-A42J-10 TCGA-2Z-A9J8-10A-01D-A42M-10 g.chr16:703789C>G c.1423C>G c.(1423-1425)Cac>Gac p.H475D KIRP 16 707787 707787 + Silent SNP C C T TCGA-P4-A5E6-01A-11D-A28G-10 TCGA-P4-A5E6-11A-22D-A28G-10 g.chr16:707787C>T c.2499C>T c.(2497-2499)ccC>ccT p.P833P KIRP 16 716291 716291 + Missense_Mutation SNP C C A TCGA-DW-7841-01A-11D-2136-08 TCGA-DW-7841-10A-01D-2136-08 g.chr16:716291C>A c.4681C>A c.(4681-4683)Cgt>Agt p.R1561S LGG 16 705148 705148 + Splice_Site SNP G G A TCGA-QH-A86X-01A-11D-A36O-08 TCGA-QH-A86X-10A-01D-A367-08 g.chr16:705148G>A c.e14+1 LGG 16 705313 705313 + Silent SNP G G A TCGA-E1-A7YM-01A-11D-A34A-08 TCGA-E1-A7YM-10A-01D-A34A-08 g.chr16:705313G>A c.1563G>A c.(1561-1563)gcG>gcA p.A521A LGG 16 709106 709106 + Frame_Shift_Del DEL C C - TCGA-HT-8105-01A-11D-2395-08 TCGA-HT-8105-10A-01D-2396-08 g.chr16:709106delC c.3032delC c.(3031-3033)gccfs p.A1011fs LGG 16 716482 716482 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:716482G>T c.4768G>T c.(4768-4770)Gac>Tac p.D1590Y LIHC 16 699822 699822 + Missense_Mutation SNP T T C TCGA-BC-A3KF-01A-11D-A20W-10 TCGA-BC-A3KF-10A-01D-A20W-10 g.chr16:699822T>C c.70T>C c.(70-72)Tcc>Ccc p.S24P LIHC 16 701923 701923 + Missense_Mutation SNP A A C TCGA-5C-AAPD-01A-21D-A38X-10 TCGA-5C-AAPD-10A-01D-A38X-10 g.chr16:701923A>C c.937A>C c.(937-939)Agc>Cgc p.S313R LIHC 16 705305 705305 + Splice_Site SNP A A G TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr16:705305A>G c.e15-1 LIHC 16 706396 706396 + Silent SNP G G A TCGA-2Y-A9H8-01A-11D-A38X-10 TCGA-2Y-A9H8-10A-01D-A38X-10 g.chr16:706396G>A c.2061G>A c.(2059-2061)acG>acA p.T687T LIHC 16 709346 709346 + Missense_Mutation SNP G G A TCGA-UB-A7MD-01A-12D-A34Z-10 TCGA-UB-A7MD-10A-01D-A34Z-10 g.chr16:709346G>A c.3154G>A c.(3154-3156)Gtc>Atc p.V1052I LIHC 16 711769 711769 + Silent SNP G G T TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr16:711769G>T c.3846G>T c.(3844-3846)ggG>ggT p.G1282G LIHC 16 712038 712038 + Nonsense_Mutation SNP G G T TCGA-DD-AADV-01A-11D-A38X-10 TCGA-DD-AADV-10A-01D-A38X-10 g.chr16:712038G>T c.4012G>T c.(4012-4014)Gag>Tag p.E1338* LIHC 16 717526 717526 + Silent SNP C C T TCGA-DD-AAVW-01A-11D-A40R-10 TCGA-DD-AAVW-10A-01D-A40U-10 g.chr16:717526C>T c.5184C>T c.(5182-5184)tcC>tcT p.S1728S LUAD 16 700152 700152 + Silent SNP C C G TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr16:700152C>G c.264C>G c.(262-264)ctC>ctG p.L88L LUAD 16 700343 700343 + Missense_Mutation SNP G G T TCGA-44-6144-01A-11D-1753-08 TCGA-44-6144-10A-01D-1753-08 g.chr16:700343G>T c.369G>T c.(367-369)gaG>gaT p.E123D LUAD 16 701983 701983 + Missense_Mutation SNP C C A TCGA-64-5779-01A-01D-1625-08 TCGA-64-5779-10A-01D-1625-08 g.chr16:701983C>A c.997C>A c.(997-999)Cac>Aac p.H333N LUAD 16 705095 705095 + Missense_Mutation SNP C C T TCGA-69-8254-01A-11D-2284-08 TCGA-69-8254-10A-01D-2284-08 g.chr16:705095C>T c.1504C>T c.(1504-1506)Cac>Tac p.H502Y LUAD 16 705355 705355 + Silent SNP C C T TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chr16:705355C>T c.1605C>T c.(1603-1605)ggC>ggT p.G535G LUAD 16 705382 705382 + Silent SNP C C T TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr16:705382C>T c.1632C>T c.(1630-1632)gaC>gaT p.D544D LUAD 16 706348 706348 + Silent SNP C C T TCGA-44-6777-01A-11D-1855-08 TCGA-44-6777-10A-01D-1855-08 g.chr16:706348C>T c.2013C>T c.(2011-2013)ctC>ctT p.L671L LUAD 16 706405 706405 + Silent SNP G G T TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr16:706405G>T c.2070G>T c.(2068-2070)cgG>cgT p.R690R LUAD 16 706454 706454 + Missense_Mutation SNP G G T TCGA-97-8176-01A-11D-2393-08 TCGA-97-8176-10B-01D-2393-08 g.chr16:706454G>T c.2119G>T c.(2119-2121)Gcc>Tcc p.A707S LUAD 16 708613 708613 + Missense_Mutation SNP A A G TCGA-05-4389-01A-01D-1265-08 TCGA-05-4389-10A-01D-1265-08 g.chr16:708613A>G c.2855A>G c.(2854-2856)aAg>aGg p.K952R LUAD 16 709087 709087 + Splice_Site SNP G G A TCGA-62-A472-01A-11D-A24D-08 TCGA-62-A472-10A-01D-A24F-08 g.chr16:709087G>A c.3013G>A c.(3013-3015)Gac>Aac p.D1005N LUAD 16 711452 711452 + Silent SNP C C T TCGA-99-8032-01A-11D-2238-08 TCGA-99-8032-10A-01D-2238-08 g.chr16:711452C>T c.3624C>T c.(3622-3624)acC>acT p.T1208T LUAD 16 712009 712019 + Frame_Shift_Del DEL CGCGTGCCGGC CGCGTGCCGGC - TCGA-97-8179-01A-11D-2284-08 TCGA-97-8179-10A-01D-2284-08 g.chr16:712009_712019delCGCGTGCCGGC c.3983_3993delCGCGTGCCGGC c.(3982-3993)acgcgtgccggcfs p.TRAG1328fs LUAD 16 712698 712698 + Missense_Mutation SNP G G A TCGA-55-7724-01A-11D-2167-08 TCGA-55-7724-10A-01D-2167-08 g.chr16:712698G>A c.4165G>A c.(4165-4167)Gag>Aag p.E1389K LUAD 16 712767 712767 + Missense_Mutation SNP A A T TCGA-64-5778-01A-01D-1625-08 TCGA-64-5778-10A-01D-1625-08 g.chr16:712767A>T c.4234A>T c.(4234-4236)Acc>Tcc p.T1412S LUAD 16 715997 715997 + Silent SNP G G A TCGA-64-1676-01A-01D-0969-08 TCGA-64-1676-10A-01D-0969-08 g.chr16:715997G>A c.4482G>A c.(4480-4482)gaG>gaA p.E1494E LUAD 16 716315 716315 + Missense_Mutation SNP G G T TCGA-50-5931-01A-11D-1753-08 TCGA-50-5931-11A-01D-1753-08 g.chr16:716315G>T c.4705G>T c.(4705-4707)Gcc>Tcc p.A1569S LUAD 16 716508 716508 + Missense_Mutation SNP C C G TCGA-75-5122-01A-01D-1753-08 TCGA-75-5122-10A-01D-1753-08 g.chr16:716508C>G c.4794C>G c.(4792-4794)gaC>gaG p.D1598E LUAD 16 716515 716515 + Missense_Mutation SNP G G T TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr16:716515G>T c.4801G>T c.(4801-4803)Gtc>Ttc p.V1601F LUAD 16 716792 716792 + Splice_Site SNP G G T TCGA-55-6642-01A-11D-1855-08 TCGA-55-6642-11A-01D-1855-08 g.chr16:716792G>T c.5004G>T c.(5002-5004)caG>caT p.Q1668H LUAD 16 716793 716793 + Splice_Site SNP G G T TCGA-55-6642-01A-11D-1855-08 TCGA-55-6642-11A-01D-1855-08 g.chr16:716793G>T c.e39+1 LUAD 16 716961 716961 + Silent SNP G G T TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr16:716961G>T c.5061G>T c.(5059-5061)ggG>ggT p.G1687G LUSC 16 703577 703577 + Missense_Mutation SNP C C A TCGA-22-5472-01A-01D-1632-08 TCGA-22-5472-11A-11D-1632-08 g.chr16:703577C>A c.1286C>A c.(1285-1287)gCa>gAa p.A429E LUSC 16 705883 705883 + Missense_Mutation SNP G G A TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr16:705883G>A c.1960G>A c.(1960-1962)Gag>Aag p.E654K LUSC 16 708258 708258 + Missense_Mutation SNP C C T TCGA-37-4133-01A-01D-1352-08 TCGA-37-4133-10A-01D-1352-08 g.chr16:708258C>T c.2680C>T c.(2680-2682)Cct>Tct p.P894S LUSC 16 708597 708597 + Missense_Mutation SNP G G T TCGA-37-4135-01A-01D-1352-08 TCGA-37-4135-10A-01D-1352-08 g.chr16:708597G>T c.2839G>T c.(2839-2841)Gcc>Tcc p.A947S LUSC 16 711941 711941 + Silent SNP G G C TCGA-18-3410-01A-01D-0983-08 TCGA-18-3410-11A-01D-0983-08 g.chr16:711941G>C c.3915G>C c.(3913-3915)tcG>tcC p.S1305S LUSC 16 712030 712030 + Missense_Mutation SNP T T C TCGA-34-5240-01A-01D-1441-08 TCGA-34-5240-10A-01D-1441-08 g.chr16:712030T>C c.4004T>C c.(4003-4005)tTg>tCg p.L1335S LUSC 16 716485 716485 + Missense_Mutation SNP C C G TCGA-39-5027-01A-21D-1817-08 TCGA-39-5027-11A-01D-1817-08 g.chr16:716485C>G c.4771C>G c.(4771-4773)Cta>Gta p.L1591V OV 16 705065 705065 + Missense_Mutation SNP G G A TCGA-13-1504-01A-01W-0545-08 TCGA-13-1504-10A-01W-0546-08 g.chr16:705065G>A c.1474G>A c.(1474-1476)Ggt>Agt p.G492S PAAD 16 701015 701015 + Missense_Mutation SNP G G A TCGA-FB-AAQ2-01A-31D-A40W-08 TCGA-FB-AAQ2-11A-11D-A40W-08 g.chr16:701015G>A c.580G>A c.(580-582)Gca>Aca p.A194T PAAD 16 701862 701862 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:701862G>A c.876G>A c.(874-876)ccG>ccA p.P292P PAAD 16 702503 702503 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:702503G>A c.1090G>A c.(1090-1092)Gtc>Atc p.V364I PAAD 16 703653 703653 + Silent SNP C C T TCGA-HV-A7OL-01A-11D-A33T-08 TCGA-HV-A7OL-10A-01D-A33W-08 g.chr16:703653C>T c.1362C>T c.(1360-1362)caC>caT p.H454H PAAD 16 705640 705640 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:705640C>A c.1786C>A c.(1786-1788)Cgc>Agc p.R596S PAAD 16 708580 708580 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:708580G>A c.2822G>A c.(2821-2823)cGc>cAc p.R941H PAAD 16 708595 708595 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:708595C>A c.2837C>A c.(2836-2838)gCc>gAc p.A946D PAAD 16 708985 708985 + Silent SNP C C G TCGA-3A-A9J0-01A-11D-A40W-08 TCGA-3A-A9J0-10A-01D-A40W-08 g.chr16:708985C>G c.2985C>G c.(2983-2985)ctC>ctG p.L995L PAAD 16 709106 709106 + Frame_Shift_Del DEL C C - TCGA-3A-A9I9-01A-11D-A38G-08 TCGA-3A-A9I9-10A-01D-A38J-08 g.chr16:709106delC c.3032delC c.(3031-3033)gccfs p.A1011fs PAAD 16 711075 711075 + Missense_Mutation SNP G G A TCGA-US-A77G-01A-11D-A32N-08 TCGA-US-A77G-11A-11D-A32N-08 g.chr16:711075G>A c.3416G>A c.(3415-3417)cGc>cAc p.R1139H PRAD 16 703426 703426 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:703426G>A c.1208G>A c.(1207-1209)cGc>cAc p.R403H PRAD 16 703785 703785 + Silent SNP G G A TCGA-EJ-7783-01A-11D-2114-08 TCGA-EJ-7783-10A-01D-2114-08 g.chr16:703785G>A c.1419G>A c.(1417-1419)aaG>aaA p.K473K PRAD 16 708965 708965 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:708965G>A c.2965G>A c.(2965-2967)Gca>Aca p.A989T SKCM 16 700084 700084 + Missense_Mutation SNP G G A TCGA-EE-A180-06A-11D-A21A-08 TCGA-EE-A180-10B-01D-A21A-08 g.chr16:700084G>A c.196G>A c.(196-198)Ggg>Agg p.G66R SKCM 16 700291 700291 + Missense_Mutation SNP T T G TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr16:700291T>G c.317T>G c.(316-318)tTc>tGc p.F106C SKCM 16 701848 701848 + Missense_Mutation SNP C C T TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chr16:701848C>T c.862C>T c.(862-864)Ccc>Tcc p.P288S SKCM 16 703431 703431 + Missense_Mutation SNP T T C TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr16:703431T>C c.1213T>C c.(1213-1215)Ttc>Ctc p.F405L SKCM 16 705079 705079 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:705079C>T c.1488C>T c.(1486-1488)gtC>gtT p.V496V SKCM 16 705369 705369 + Missense_Mutation SNP C C T TCGA-D3-A2JG-06A-11D-A196-08 TCGA-D3-A2JG-10A-01D-A198-08 g.chr16:705369C>T c.1619C>T c.(1618-1620)tCc>tTc p.S540F SKCM 16 706315 706315 + Silent SNP C C G TCGA-ER-A19D-06A-11D-A197-08 TCGA-ER-A19D-10A-01D-A199-08 g.chr16:706315C>G c.1980C>G c.(1978-1980)ccC>ccG p.P660P SKCM 16 706315 706315 + Silent SNP C C T TCGA-DA-A1I5-06A-11D-A197-08 TCGA-DA-A1I5-10A-01D-A199-08 g.chr16:706315C>T c.1980C>T c.(1978-1980)ccC>ccT p.P660P SKCM 16 706349 706349 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr16:706349C>T c.2014C>T c.(2014-2016)Cgt>Tgt p.R672C SKCM 16 708548 708548 + Silent SNP C C T TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr16:708548C>T c.2790C>T c.(2788-2790)ccC>ccT p.P930P SKCM 16 708645 708645 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:708645G>A c.2887G>A c.(2887-2889)Ggc>Agc p.G963S SKCM 16 709106 709106 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr16:709106C>T c.3032C>T c.(3031-3033)gCc>gTc p.A1011V SKCM 16 709107 709107 + Silent SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr16:709107C>T c.3033C>T c.(3031-3033)gcC>gcT p.A1011A SKCM 16 711461 711461 + Silent SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr16:711461C>T c.3633C>T c.(3631-3633)gcC>gcT p.A1211A SKCM 16 716084 716084 + Silent SNP C C T TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr16:716084C>T c.4569C>T c.(4567-4569)ccC>ccT p.P1523P SKCM 16 716085 716085 + Missense_Mutation SNP C C T TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr16:716085C>T c.4570C>T c.(4570-4572)Cac>Tac p.H1524Y SKCM 16 716594 716594 + Missense_Mutation SNP C C T TCGA-EE-A2A6-06A-11D-A197-08 TCGA-EE-A2A6-10A-01D-A199-08 g.chr16:716594C>T c.4880C>T c.(4879-4881)aCg>aTg p.T1627M SKCM 16 716717 716717 + Nonsense_Mutation SNP G G A TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr16:716717G>A c.4929G>A c.(4927-4929)tgG>tgA p.W1643* SKCM 16 716970 716970 + Silent SNP C C T TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr16:716970C>T c.5070C>T c.(5068-5070)ctC>ctT p.L1690L SKCM 16 717536 717536 + Missense_Mutation SNP C C T TCGA-DA-A1IA-06A-11D-A196-08 TCGA-DA-A1IA-10A-01D-A198-08 g.chr16:717536C>T c.5194C>T c.(5194-5196)Ctc>Ttc p.L1732F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 16 720501 720501 single base substitution G A downstream_gene_variant AML-US 16 703576 703576 single base substitution G T downstream_gene_variant AML-US 16 703576 703576 single base substitution G T exon_variant AML-US 16 703576 703576 single base substitution G T missense_variant A429S 1285G>T AML-US 16 703576 703576 single base substitution G T upstream_gene_variant BLCA-CN 16 708255 708255 single base substitution G C downstream_gene_variant BLCA-CN 16 708255 708255 single base substitution G C exon_variant BLCA-CN 16 708255 708255 single base substitution G C missense_variant G893R 2677G>C BLCA-CN 16 708255 708255 single base substitution G C upstream_gene_variant BLCA-CN 16 716502 716502 single base substitution T G 3_prime_UTR_variant BLCA-CN 16 716502 716502 single base substitution T G downstream_gene_variant BLCA-CN 16 716502 716502 single base substitution T G exon_variant BLCA-CN 16 716502 716502 single base substitution T G intron_variant BLCA-CN 16 716502 716502 single base substitution T G missense_variant S1596R 4788T>G BLCA-CN 16 716502 716502 single base substitution T G missense_variant S1598R 4794T>G BLCA-CN 16 716502 716502 single base substitution T G missense_variant S195R 585T>G BLCA-CN 16 716502 716502 single base substitution T G missense_variant S2R 6T>G BLCA-CN 16 716502 716502 single base substitution T G upstream_gene_variant BLCA-CN 16 716676 716676 single base substitution C A 3_prime_UTR_variant BLCA-CN 16 716676 716676 single base substitution C A downstream_gene_variant BLCA-CN 16 716676 716676 single base substitution C A exon_variant BLCA-CN 16 716676 716676 single base substitution C A missense_variant Q1630K 4888C>A BLCA-CN 16 716676 716676 single base substitution C A missense_variant Q1632K 4894C>A BLCA-CN 16 716676 716676 single base substitution C A missense_variant Q181K 541C>A BLCA-CN 16 716676 716676 single base substitution C A missense_variant Q229K 685C>A BLCA-CN 16 716676 716676 single base substitution C A missense_variant Q36K 106C>A BLCA-CN 16 716676 716676 single base substitution C A upstream_gene_variant BLCA-CN 16 717556 717556 single base substitution C A 3_prime_UTR_variant BLCA-CN 16 717556 717556 single base substitution C A downstream_gene_variant BLCA-CN 16 717556 717556 single base substitution C A exon_variant BLCA-CN 16 717556 717556 single base substitution C A missense_variant N1738K 5214C>A BLCA-CN 16 717556 717556 single base substitution C A missense_variant N1740K 5220C>A BLCA-CN 16 717556 717556 single base substitution C A missense_variant N289K 867C>A BLCA-CN 16 717556 717556 single base substitution C A missense_variant N337K 1011C>A BLCA-CN 16 717556 717556 single base substitution C A missense_variant T41K 122C>A BLCA-CN 16 720746 720746 single base substitution C G downstream_gene_variant BLCA-CN 16 720960 720960 single base substitution C T downstream_gene_variant BLCA-US 16 697470 697470 single base substitution C T upstream_gene_variant BLCA-US 16 697532 697532 single base substitution T A upstream_gene_variant BLCA-US 16 700002 700002 single base substitution G A exon_variant BLCA-US 16 700002 700002 single base substitution G A synonymous_variant L38L 114G>A BLCA-US 16 700002 700002 single base substitution G A upstream_gene_variant BLCA-US 16 703599 703599 single base substitution G A downstream_gene_variant BLCA-US 16 703599 703599 single base substitution G A exon_variant BLCA-US 16 703599 703599 single base substitution G A synonymous_variant R436R 1308G>A BLCA-US 16 703599 703599 single base substitution G A upstream_gene_variant BLCA-US 16 703802 703802 single base substitution C T downstream_gene_variant BLCA-US 16 703802 703802 single base substitution C T exon_variant BLCA-US 16 703802 703802 single base substitution C T missense_variant T479M 1436C>T BLCA-US 16 703802 703802 single base substitution C T splice_region_variant BLCA-US 16 703802 703802 single base substitution C T upstream_gene_variant BLCA-US 16 708543 708543 single base substitution G A downstream_gene_variant BLCA-US 16 708543 708543 single base substitution G A exon_variant BLCA-US 16 708543 708543 single base substitution G A missense_variant E929K 2785G>A BLCA-US 16 708543 708543 single base substitution G A upstream_gene_variant BLCA-US 16 716290 716290 single base substitution C T 3_prime_UTR_variant BLCA-US 16 716290 716290 single base substitution C T downstream_gene_variant BLCA-US 16 716290 716290 single base substitution C T exon_variant BLCA-US 16 716290 716290 single base substitution C T synonymous_variant F1560F 4680C>T BLCA-US 16 716290 716290 single base substitution C T synonymous_variant F1562F 4686C>T BLCA-US 16 716290 716290 single base substitution C T synonymous_variant F159F 477C>T BLCA-US 16 716290 716290 single base substitution C T upstream_gene_variant BLCA-US 16 716521 716521 single base substitution G T 3_prime_UTR_variant BLCA-US 16 716521 716521 single base substitution G T downstream_gene_variant BLCA-US 16 716521 716521 single base substitution G T exon_variant BLCA-US 16 716521 716521 single base substitution G T intron_variant BLCA-US 16 716521 716521 single base substitution G T missense_variant V1603F 4807G>T BLCA-US 16 716521 716521 single base substitution G T missense_variant V1605F 4813G>T BLCA-US 16 716521 716521 single base substitution G T missense_variant V202F 604G>T BLCA-US 16 716521 716521 single base substitution G T missense_variant V9F 25G>T BLCA-US 16 716521 716521 single base substitution G T upstream_gene_variant BOCA-FR 16 705620 705620 single base substitution G A downstream_gene_variant BOCA-FR 16 705620 705620 single base substitution G A exon_variant BOCA-FR 16 705620 705620 single base substitution G A missense_variant R589H 1766G>A BOCA-FR 16 705620 705620 single base substitution G A upstream_gene_variant BRCA-EU 16 695157 695157 single base substitution C T upstream_gene_variant BRCA-EU 16 695165 695165 single base substitution T G upstream_gene_variant BRCA-EU 16 695848 695848 single base substitution C T upstream_gene_variant BRCA-EU 16 696736 696736 single base substitution C T upstream_gene_variant BRCA-EU 16 698732 698732 single base substitution G C upstream_gene_variant BRCA-EU 16 699252 699252 single base substitution A C upstream_gene_variant BRCA-EU 16 700475 700475 single base substitution C G intron_variant BRCA-EU 16 700475 700475 single base substitution C G upstream_gene_variant BRCA-EU 16 700757 700757 single base substitution C G intron_variant BRCA-EU 16 700757 700757 single base substitution C G upstream_gene_variant BRCA-EU 16 701285 701285 single base substitution C T intron_variant BRCA-EU 16 701285 701285 single base substitution C T upstream_gene_variant BRCA-EU 16 704616 704616 deletion of <=200bp T - downstream_gene_variant BRCA-EU 16 704616 704616 deletion of <=200bp T - exon_variant BRCA-EU 16 704616 704616 deletion of <=200bp T - intron_variant BRCA-EU 16 704616 704616 deletion of <=200bp T - upstream_gene_variant BRCA-EU 16 706065 706065 single base substitution G A downstream_gene_variant BRCA-EU 16 706065 706065 single base substitution G A exon_variant BRCA-EU 16 706065 706065 single base substitution G A intron_variant BRCA-EU 16 706065 706065 single base substitution G A upstream_gene_variant BRCA-EU 16 707514 707514 single base substitution G C downstream_gene_variant BRCA-EU 16 707514 707514 single base substitution G C intron_variant BRCA-EU 16 707514 707514 single base substitution G C upstream_gene_variant BRCA-EU 16 707849 707849 single base substitution C T downstream_gene_variant BRCA-EU 16 707849 707849 single base substitution C T exon_variant BRCA-EU 16 707849 707849 single base substitution C T missense_variant S854F 2561C>T BRCA-EU 16 707849 707849 single base substitution C T upstream_gene_variant BRCA-EU 16 708207 708207 single base substitution C G downstream_gene_variant BRCA-EU 16 708207 708207 single base substitution C G exon_variant BRCA-EU 16 708207 708207 single base substitution C G missense_variant L877V 2629C>G BRCA-EU 16 708207 708207 single base substitution C G upstream_gene_variant BRCA-EU 16 709272 709272 single base substitution C T downstream_gene_variant BRCA-EU 16 709272 709272 single base substitution C T exon_variant BRCA-EU 16 709272 709272 single base substitution C T missense_variant A1027V 3080C>T BRCA-EU 16 709272 709272 single base substitution C T missense_variant A9V 26C>T BRCA-EU 16 709272 709272 single base substitution C T upstream_gene_variant BRCA-EU 16 709599 709599 single base substitution C G downstream_gene_variant BRCA-EU 16 709599 709599 single base substitution C G intron_variant BRCA-EU 16 709599 709599 single base substitution C G upstream_gene_variant BRCA-EU 16 710185 710185 single base substitution C T downstream_gene_variant BRCA-EU 16 710185 710185 single base substitution C T intron_variant BRCA-EU 16 710185 710185 single base substitution C T upstream_gene_variant BRCA-EU 16 710389 710389 single base substitution C A downstream_gene_variant BRCA-EU 16 710389 710389 single base substitution C A intron_variant BRCA-EU 16 710389 710389 single base substitution C A upstream_gene_variant BRCA-EU 16 711052 711052 single base substitution C T downstream_gene_variant BRCA-EU 16 711052 711052 single base substitution C T splice_region_variant BRCA-EU 16 711052 711052 single base substitution C T upstream_gene_variant BRCA-EU 16 712009 712009 single base substitution C T 3_prime_UTR_variant BRCA-EU 16 712009 712009 single base substitution C T downstream_gene_variant BRCA-EU 16 712009 712009 single base substitution C T exon_variant BRCA-EU 16 712009 712009 single base substitution C T missense_variant T1328M 3983C>T BRCA-EU 16 712009 712009 single base substitution C T upstream_gene_variant BRCA-EU 16 712963 712963 single base substitution G A downstream_gene_variant BRCA-EU 16 712963 712963 single base substitution G A exon_variant BRCA-EU 16 712963 712963 single base substitution G A intron_variant BRCA-EU 16 712963 712963 single base substitution G A upstream_gene_variant BRCA-EU 16 713734 713738 deletion of <=200bp TCATG - downstream_gene_variant BRCA-EU 16 713734 713738 deletion of <=200bp TCATG - intron_variant BRCA-EU 16 713734 713738 deletion of <=200bp TCATG - upstream_gene_variant BRCA-EU 16 715674 715674 single base substitution C T downstream_gene_variant BRCA-EU 16 715674 715674 single base substitution C T exon_variant BRCA-EU 16 715674 715674 single base substitution C T missense_variant P35L 104C>T BRCA-EU 16 715674 715674 single base substitution C T splice_region_variant BRCA-EU 16 715674 715674 single base substitution C T upstream_gene_variant BRCA-EU 16 715973 715973 single base substitution C G 3_prime_UTR_variant BRCA-EU 16 715973 715973 single base substitution C G downstream_gene_variant BRCA-EU 16 715973 715973 single base substitution C G exon_variant BRCA-EU 16 715973 715973 single base substitution C G missense_variant S1486R 4458C>G BRCA-EU 16 715973 715973 single base substitution C G missense_variant S1488R 4464C>G BRCA-EU 16 715973 715973 single base substitution C G missense_variant S85R 255C>G BRCA-EU 16 715973 715973 single base substitution C G upstream_gene_variant BRCA-EU 16 716118 716118 single base substitution A T 3_prime_UTR_variant BRCA-EU 16 716118 716118 single base substitution A T downstream_gene_variant BRCA-EU 16 716118 716118 single base substitution A T exon_variant BRCA-EU 16 716118 716118 single base substitution A T missense_variant T134S 400A>T BRCA-EU 16 716118 716118 single base substitution A T missense_variant T1535S 4603A>T BRCA-EU 16 716118 716118 single base substitution A T missense_variant T1537S 4609A>T BRCA-EU 16 716118 716118 single base substitution A T upstream_gene_variant BRCA-EU 16 718067 718067 single base substitution G C downstream_gene_variant BRCA-EU 16 719130 719130 single base substitution C A downstream_gene_variant BRCA-EU 16 720869 720869 single base substitution C A downstream_gene_variant BRCA-FR 16 696655 696655 single base substitution C G upstream_gene_variant BRCA-FR 16 696983 696983 single base substitution G A upstream_gene_variant BRCA-FR 16 699252 699252 single base substitution A C upstream_gene_variant BRCA-FR 16 707213 707213 single base substitution G C downstream_gene_variant BRCA-FR 16 707213 707213 single base substitution G C exon_variant BRCA-FR 16 707213 707213 single base substitution G C missense_variant R822P 2465G>C BRCA-FR 16 707213 707213 single base substitution G C upstream_gene_variant BRCA-FR 16 713023 713023 single base substitution C A downstream_gene_variant BRCA-FR 16 713023 713023 single base substitution C A exon_variant BRCA-FR 16 713023 713023 single base substitution C A intron_variant BRCA-FR 16 713023 713023 single base substitution C A upstream_gene_variant BRCA-FR 16 715718 715718 single base substitution G A 3_prime_UTR_variant BRCA-FR 16 715718 715718 single base substitution G A downstream_gene_variant BRCA-FR 16 715718 715718 single base substitution G A exon_variant BRCA-FR 16 715718 715718 single base substitution G A missense_variant A1451T 4351G>A BRCA-FR 16 715718 715718 single base substitution G A missense_variant A1453T 4357G>A BRCA-FR 16 715718 715718 single base substitution G A missense_variant A50T 148G>A BRCA-FR 16 715718 715718 single base substitution G A upstream_gene_variant BRCA-KR 16 720486 720486 single base substitution G C downstream_gene_variant BRCA-UK 16 694636 694636 single base substitution C T upstream_gene_variant BRCA-US 16 701847 701847 single base substitution A C exon_variant BRCA-US 16 701847 701847 single base substitution A C synonymous_variant A287A 861A>C BRCA-US 16 701847 701847 single base substitution A C upstream_gene_variant BRCA-US 16 705776 705776 single base substitution C T downstream_gene_variant BRCA-US 16 705776 705776 single base substitution C T exon_variant BRCA-US 16 705776 705776 single base substitution C T missense_variant P618L 1853C>T BRCA-US 16 705776 705776 single base substitution C T upstream_gene_variant BRCA-US 16 708527 708527 single base substitution G A downstream_gene_variant BRCA-US 16 708527 708527 single base substitution G A splice_region_variant BRCA-US 16 708527 708527 single base substitution G A upstream_gene_variant BRCA-US 16 709364 709364 single base substitution G A downstream_gene_variant BRCA-US 16 709364 709364 single base substitution G A exon_variant BRCA-US 16 709364 709364 single base substitution G A missense_variant E1058K 3172G>A BRCA-US 16 709364 709364 single base substitution G A missense_variant E40K 118G>A BRCA-US 16 709364 709364 single base substitution G A upstream_gene_variant BRCA-US 16 711733 711733 single base substitution G A 3_prime_UTR_variant BRCA-US 16 711733 711733 single base substitution G A downstream_gene_variant BRCA-US 16 711733 711733 single base substitution G A exon_variant BRCA-US 16 711733 711733 single base substitution G A synonymous_variant Q1270Q 3810G>A BRCA-US 16 711733 711733 single base substitution G A upstream_gene_variant BRCA-US 16 715685 715685 single base substitution G A 3_prime_UTR_variant BRCA-US 16 715685 715685 single base substitution G A downstream_gene_variant BRCA-US 16 715685 715685 single base substitution G A exon_variant BRCA-US 16 715685 715685 single base substitution G A missense_variant E1440K 4318G>A BRCA-US 16 715685 715685 single base substitution G A missense_variant E1442K 4324G>A BRCA-US 16 715685 715685 single base substitution G A missense_variant E39K 115G>A BRCA-US 16 715685 715685 single base substitution G A upstream_gene_variant BTCA-JP 16 700120 700120 single base substitution C T exon_variant BTCA-JP 16 700120 700120 single base substitution C T missense_variant P78S 232C>T BTCA-JP 16 700120 700120 single base substitution C T upstream_gene_variant BTCA-JP 16 701763 701763 single base substitution G A intron_variant BTCA-JP 16 701763 701763 single base substitution G A upstream_gene_variant BTCA-JP 16 701862 701862 single base substitution G A exon_variant BTCA-JP 16 701862 701862 single base substitution G A synonymous_variant P292P 876G>A BTCA-JP 16 701862 701862 single base substitution G A upstream_gene_variant BTCA-JP 16 702386 702386 single base substitution G T exon_variant BTCA-JP 16 702386 702386 single base substitution G T intron_variant BTCA-JP 16 702386 702386 single base substitution G T upstream_gene_variant BTCA-JP 16 702550 702550 single base substitution G A intron_variant BTCA-JP 16 702550 702550 single base substitution G A upstream_gene_variant BTCA-JP 16 705873 705873 single base substitution G T downstream_gene_variant BTCA-JP 16 705873 705873 single base substitution G T exon_variant BTCA-JP 16 705873 705873 single base substitution G T synonymous_variant S650S 1950G>T BTCA-JP 16 705873 705873 single base substitution G T upstream_gene_variant BTCA-JP 16 705889 705889 single base substitution G A downstream_gene_variant BTCA-JP 16 705889 705889 single base substitution G A exon_variant BTCA-JP 16 705889 705889 single base substitution G A missense_variant E656K 1966G>A BTCA-JP 16 705889 705889 single base substitution G A splice_region_variant BTCA-JP 16 705889 705889 single base substitution G A upstream_gene_variant BTCA-JP 16 706886 706886 deletion of <=200bp G - downstream_gene_variant BTCA-JP 16 706886 706886 deletion of <=200bp G - intron_variant BTCA-JP 16 706886 706886 deletion of <=200bp G - upstream_gene_variant BTCA-JP 16 708081 708081 single base substitution T C downstream_gene_variant BTCA-JP 16 708081 708081 single base substitution T C intron_variant BTCA-JP 16 708081 708081 single base substitution T C upstream_gene_variant BTCA-JP 16 708925 708925 single base substitution G A downstream_gene_variant BTCA-JP 16 708925 708925 single base substitution G A exon_variant BTCA-JP 16 708925 708925 single base substitution G A synonymous_variant Q975Q 2925G>A BTCA-JP 16 708925 708925 single base substitution G A upstream_gene_variant BTCA-JP 16 710636 710636 single base substitution G A downstream_gene_variant BTCA-JP 16 710636 710636 single base substitution G A exon_variant BTCA-JP 16 710636 710636 single base substitution G A missense_variant G107S 319G>A BTCA-JP 16 710636 710636 single base substitution G A missense_variant G1105S 3313G>A BTCA-JP 16 710636 710636 single base substitution G A upstream_gene_variant BTCA-JP 16 711520 711520 single base substitution G C downstream_gene_variant BTCA-JP 16 711520 711520 single base substitution G C intron_variant BTCA-JP 16 711520 711520 single base substitution G C upstream_gene_variant BTCA-JP 16 712120 712120 single base substitution G A downstream_gene_variant BTCA-JP 16 712120 712120 single base substitution G A intron_variant BTCA-JP 16 712120 712120 single base substitution G A upstream_gene_variant BTCA-JP 16 713103 713103 deletion of <=200bp T - downstream_gene_variant BTCA-JP 16 713103 713103 deletion of <=200bp T - exon_variant BTCA-JP 16 713103 713103 deletion of <=200bp T - intron_variant BTCA-JP 16 713103 713103 deletion of <=200bp T - upstream_gene_variant BTCA-JP 16 715633 715633 single base substitution C G downstream_gene_variant BTCA-JP 16 715633 715633 single base substitution C G exon_variant BTCA-JP 16 715633 715633 single base substitution C G intron_variant BTCA-JP 16 715633 715633 single base substitution C G synonymous_variant T21T 63C>G BTCA-JP 16 715633 715633 single base substitution C G upstream_gene_variant BTCA-JP 16 715700 715700 single base substitution C A 3_prime_UTR_variant BTCA-JP 16 715700 715700 single base substitution C A downstream_gene_variant BTCA-JP 16 715700 715700 single base substitution C A exon_variant BTCA-JP 16 715700 715700 single base substitution C A missense_variant P1445T 4333C>A BTCA-JP 16 715700 715700 single base substitution C A missense_variant P1447T 4339C>A BTCA-JP 16 715700 715700 single base substitution C A missense_variant P44T 130C>A BTCA-JP 16 715700 715700 single base substitution C A upstream_gene_variant BTCA-JP 16 715703 715703 single base substitution G A 3_prime_UTR_variant BTCA-JP 16 715703 715703 single base substitution G A downstream_gene_variant BTCA-JP 16 715703 715703 single base substitution G A exon_variant BTCA-JP 16 715703 715703 single base substitution G A missense_variant G1446R 4336G>A BTCA-JP 16 715703 715703 single base substitution G A missense_variant G1448R 4342G>A BTCA-JP 16 715703 715703 single base substitution G A missense_variant G45R 133G>A BTCA-JP 16 715703 715703 single base substitution G A upstream_gene_variant BTCA-JP 16 716291 716291 single base substitution C T 3_prime_UTR_variant BTCA-JP 16 716291 716291 single base substitution C T downstream_gene_variant BTCA-JP 16 716291 716291 single base substitution C T exon_variant BTCA-JP 16 716291 716291 single base substitution C T missense_variant R1561C 4681C>T BTCA-JP 16 716291 716291 single base substitution C T missense_variant R1563C 4687C>T BTCA-JP 16 716291 716291 single base substitution C T missense_variant R160C 478C>T BTCA-JP 16 716291 716291 single base substitution C T upstream_gene_variant BTCA-JP 16 716565 716565 single base substitution C T 3_prime_UTR_variant BTCA-JP 16 716565 716565 single base substitution C T downstream_gene_variant BTCA-JP 16 716565 716565 single base substitution C T exon_variant BTCA-JP 16 716565 716565 single base substitution C T intron_variant BTCA-JP 16 716565 716565 single base substitution C T synonymous_variant D1617D 4851C>T BTCA-JP 16 716565 716565 single base substitution C T synonymous_variant D1619D 4857C>T BTCA-JP 16 716565 716565 single base substitution C T synonymous_variant D216D 648C>T BTCA-JP 16 716565 716565 single base substitution C T synonymous_variant D23D 69C>T BTCA-JP 16 716565 716565 single base substitution C T upstream_gene_variant BTCA-JP 16 716659 716659 single base substitution C A downstream_gene_variant BTCA-JP 16 716659 716659 single base substitution C A exon_variant BTCA-JP 16 716659 716659 single base substitution C A intron_variant BTCA-JP 16 716659 716659 single base substitution C A upstream_gene_variant BTCA-JP 16 716981 716981 single base substitution G A 3_prime_UTR_variant BTCA-JP 16 716981 716981 single base substitution G A downstream_gene_variant BTCA-JP 16 716981 716981 single base substitution G A exon_variant BTCA-JP 16 716981 716981 single base substitution G A intron_variant BTCA-JP 16 716981 716981 single base substitution G A missense_variant G1694D 5081G>A BTCA-JP 16 716981 716981 single base substitution G A missense_variant G1696D 5087G>A BTCA-JP 16 716981 716981 single base substitution G A missense_variant G245D 734G>A BTCA-JP 16 716981 716981 single base substitution G A missense_variant G24D 71G>A BTCA-JP 16 716981 716981 single base substitution G A missense_variant G293D 878G>A BTCA-JP 16 720288 720288 single base substitution G A downstream_gene_variant BTCA-JP 16 720843 720843 single base substitution T C downstream_gene_variant BTCA-JP 16 721822 721822 single base substitution T G downstream_gene_variant BTCA-JP 16 722596 722596 single base substitution C A downstream_gene_variant CESC-US 16 705684 705684 single base substitution G A downstream_gene_variant CESC-US 16 705684 705684 single base substitution G A exon_variant CESC-US 16 705684 705684 single base substitution G A synonymous_variant Q610Q 1830G>A CESC-US 16 705684 705684 single base substitution G A upstream_gene_variant CESC-US 16 705701 705701 single base substitution C T downstream_gene_variant CESC-US 16 705701 705701 single base substitution C T missense_variant S616L 1847C>T CESC-US 16 705701 705701 single base substitution C T splice_region_variant CESC-US 16 705701 705701 single base substitution C T upstream_gene_variant CESC-US 16 707790 707790 single base substitution G A downstream_gene_variant CESC-US 16 707790 707790 single base substitution G A exon_variant CESC-US 16 707790 707790 single base substitution G A synonymous_variant A834A 2502G>A CESC-US 16 707790 707790 single base substitution G A upstream_gene_variant CESC-US 16 709007 709007 single base substitution G A downstream_gene_variant CESC-US 16 709007 709007 single base substitution G A exon_variant CESC-US 16 709007 709007 single base substitution G A missense_variant E1003K 3007G>A CESC-US 16 709007 709007 single base substitution G A upstream_gene_variant CESC-US 16 711352 711352 single base substitution C G downstream_gene_variant CESC-US 16 711352 711352 single base substitution C G exon_variant CESC-US 16 711352 711352 single base substitution C G missense_variant S1175C 3524C>G CESC-US 16 711352 711352 single base substitution C G upstream_gene_variant CESC-US 16 712707 712707 single base substitution C T downstream_gene_variant CESC-US 16 712707 712707 single base substitution C T exon_variant CESC-US 16 712707 712707 single base substitution C T intron_variant CESC-US 16 712707 712707 single base substitution C T synonymous_variant L1392L 4174C>T CESC-US 16 712707 712707 single base substitution C T synonymous_variant L1394L 4180C>T CESC-US 16 712707 712707 single base substitution C T upstream_gene_variant CESC-US 16 717452 717452 single base substitution G A 3_prime_UTR_variant CESC-US 16 717452 717452 single base substitution G A downstream_gene_variant CESC-US 16 717452 717452 single base substitution G A exon_variant CESC-US 16 717452 717452 single base substitution G A intron_variant CESC-US 16 717452 717452 single base substitution G A missense_variant D1704N 5110G>A CESC-US 16 717452 717452 single base substitution G A missense_variant D1706N 5116G>A CESC-US 16 717452 717452 single base substitution G A missense_variant D255N 763G>A CESC-US 16 717452 717452 single base substitution G A missense_variant D303N 907G>A CESC-US 16 720883 720883 single base substitution C T downstream_gene_variant CESC-US 16 721776 721776 single base substitution G A downstream_gene_variant CESC-US 16 722267 722267 single base substitution G C downstream_gene_variant CLLE-ES 16 698129 698129 single base substitution C G upstream_gene_variant CLLE-ES 16 703505 703505 single base substitution C T downstream_gene_variant CLLE-ES 16 703505 703505 single base substitution C T intron_variant CLLE-ES 16 703505 703505 single base substitution C T upstream_gene_variant CLLE-ES 16 707446 707446 single base substitution C T downstream_gene_variant CLLE-ES 16 707446 707446 single base substitution C T intron_variant CLLE-ES 16 707446 707446 single base substitution C T upstream_gene_variant CLLE-ES 16 714719 714719 single base substitution G C downstream_gene_variant CLLE-ES 16 714719 714719 single base substitution G C intron_variant CLLE-ES 16 714719 714719 single base substitution G C upstream_gene_variant COAD-US 16 697880 697880 single base substitution G A upstream_gene_variant COAD-US 16 701656 701656 single base substitution C T exon_variant COAD-US 16 701656 701656 single base substitution C T missense_variant P250L 749C>T COAD-US 16 701656 701656 single base substitution C T upstream_gene_variant COAD-US 16 705118 705118 single base substitution C A downstream_gene_variant COAD-US 16 705118 705118 single base substitution C A exon_variant COAD-US 16 705118 705118 single base substitution C A synonymous_variant A509A 1527C>A COAD-US 16 705118 705118 single base substitution C A upstream_gene_variant COAD-US 16 705360 705360 single base substitution T C downstream_gene_variant COAD-US 16 705360 705360 single base substitution T C exon_variant COAD-US 16 705360 705360 single base substitution T C missense_variant V537A 1610T>C COAD-US 16 705360 705360 single base substitution T C upstream_gene_variant COAD-US 16 706340 706340 single base substitution G T downstream_gene_variant COAD-US 16 706340 706340 single base substitution G T exon_variant COAD-US 16 706340 706340 single base substitution G T missense_variant D669Y 2005G>T COAD-US 16 706340 706340 single base substitution G T upstream_gene_variant COAD-US 16 706404 706404 single base substitution G A downstream_gene_variant COAD-US 16 706404 706404 single base substitution G A exon_variant COAD-US 16 706404 706404 single base substitution G A missense_variant R690Q 2069G>A COAD-US 16 706404 706404 single base substitution G A upstream_gene_variant COAD-US 16 706534 706534 single base substitution G A downstream_gene_variant COAD-US 16 706534 706534 single base substitution G A exon_variant COAD-US 16 706534 706534 single base substitution G A synonymous_variant Q733Q 2199G>A COAD-US 16 706534 706534 single base substitution G A upstream_gene_variant COAD-US 16 708275 708275 single base substitution C A downstream_gene_variant COAD-US 16 708275 708275 single base substitution C A exon_variant COAD-US 16 708275 708275 single base substitution C A missense_variant H899Q 2697C>A COAD-US 16 708275 708275 single base substitution C A upstream_gene_variant COAD-US 16 708326 708326 single base substitution G A downstream_gene_variant COAD-US 16 708326 708326 single base substitution G A exon_variant COAD-US 16 708326 708326 single base substitution G A synonymous_variant S916S 2748G>A COAD-US 16 708326 708326 single base substitution G A upstream_gene_variant COAD-US 16 708330 708330 single base substitution C T downstream_gene_variant COAD-US 16 708330 708330 single base substitution C T exon_variant COAD-US 16 708330 708330 single base substitution C T missense_variant R918C 2752C>T COAD-US 16 708330 708330 single base substitution C T upstream_gene_variant COAD-US 16 709001 709001 single base substitution C A downstream_gene_variant COAD-US 16 709001 709001 single base substitution C A exon_variant COAD-US 16 709001 709001 single base substitution C A missense_variant P1001T 3001C>A COAD-US 16 709001 709001 single base substitution C A upstream_gene_variant COAD-US 16 709106 709106 deletion of <=200bp C - downstream_gene_variant COAD-US 16 709106 709106 deletion of <=200bp C - exon_variant COAD-US 16 709106 709106 deletion of <=200bp C - frameshift_variant A1011 COAD-US 16 709106 709106 deletion of <=200bp C - upstream_gene_variant COAD-US 16 709248 709248 single base substitution C T downstream_gene_variant COAD-US 16 709248 709248 single base substitution C T exon_variant COAD-US 16 709248 709248 single base substitution C T missense_variant P1019L 3056C>T COAD-US 16 709248 709248 single base substitution C T missense_variant P1L 2C>T COAD-US 16 709248 709248 single base substitution C T upstream_gene_variant COAD-US 16 710629 710629 single base substitution C T downstream_gene_variant COAD-US 16 710629 710629 single base substitution C T exon_variant COAD-US 16 710629 710629 single base substitution C T synonymous_variant P104P 312C>T COAD-US 16 710629 710629 single base substitution C T synonymous_variant P1102P 3306C>T COAD-US 16 710629 710629 single base substitution C T upstream_gene_variant COAD-US 16 711639 711639 single base substitution C A 3_prime_UTR_variant COAD-US 16 711639 711639 single base substitution C A downstream_gene_variant COAD-US 16 711639 711639 single base substitution C A exon_variant COAD-US 16 711639 711639 single base substitution C A missense_variant T1239N 3716C>A COAD-US 16 711639 711639 single base substitution C A upstream_gene_variant COAD-US 16 711712 711712 single base substitution C T 3_prime_UTR_variant COAD-US 16 711712 711712 single base substitution C T downstream_gene_variant COAD-US 16 711712 711712 single base substitution C T exon_variant COAD-US 16 711712 711712 single base substitution C T synonymous_variant G1263G 3789C>T COAD-US 16 711712 711712 single base substitution C T upstream_gene_variant COAD-US 16 711905 711905 single base substitution A G 3_prime_UTR_variant COAD-US 16 711905 711905 single base substitution A G downstream_gene_variant COAD-US 16 711905 711905 single base substitution A G exon_variant COAD-US 16 711905 711905 single base substitution A G synonymous_variant P1293P 3879A>G COAD-US 16 711905 711905 single base substitution A G upstream_gene_variant COAD-US 16 711950 711950 single base substitution C T 3_prime_UTR_variant COAD-US 16 711950 711950 single base substitution C T downstream_gene_variant COAD-US 16 711950 711950 single base substitution C T exon_variant COAD-US 16 711950 711950 single base substitution C T synonymous_variant Y1308Y 3924C>T COAD-US 16 711950 711950 single base substitution C T upstream_gene_variant COAD-US 16 712760 712760 single base substitution C T downstream_gene_variant COAD-US 16 712760 712760 single base substitution C T exon_variant COAD-US 16 712760 712760 single base substitution C T intron_variant COAD-US 16 712760 712760 single base substitution C T synonymous_variant V1409V 4227C>T COAD-US 16 712760 712760 single base substitution C T synonymous_variant V1411V 4233C>T COAD-US 16 712760 712760 single base substitution C T upstream_gene_variant COAD-US 16 715990 715990 single base substitution G A 3_prime_UTR_variant COAD-US 16 715990 715990 single base substitution G A downstream_gene_variant COAD-US 16 715990 715990 single base substitution G A exon_variant COAD-US 16 715990 715990 single base substitution G A missense_variant R1492H 4475G>A COAD-US 16 715990 715990 single base substitution G A missense_variant R1494H 4481G>A COAD-US 16 715990 715990 single base substitution G A missense_variant R91H 272G>A COAD-US 16 715990 715990 single base substitution G A upstream_gene_variant COAD-US 16 716059 716059 single base substitution C T 3_prime_UTR_variant COAD-US 16 716059 716059 single base substitution C T downstream_gene_variant COAD-US 16 716059 716059 single base substitution C T exon_variant COAD-US 16 716059 716059 single base substitution C T missense_variant T114M 341C>T COAD-US 16 716059 716059 single base substitution C T missense_variant T1515M 4544C>T COAD-US 16 716059 716059 single base substitution C T missense_variant T1517M 4550C>T COAD-US 16 716059 716059 single base substitution C T upstream_gene_variant COAD-US 16 717523 717523 single base substitution G T 3_prime_UTR_variant COAD-US 16 717523 717523 single base substitution G T downstream_gene_variant COAD-US 16 717523 717523 single base substitution G T exon_variant COAD-US 16 717523 717523 single base substitution G T missense_variant R30L 89G>T COAD-US 16 717523 717523 single base substitution G T synonymous_variant P1727P 5181G>T COAD-US 16 717523 717523 single base substitution G T synonymous_variant P1729P 5187G>T COAD-US 16 717523 717523 single base substitution G T synonymous_variant P278P 834G>T COAD-US 16 717523 717523 single base substitution G T synonymous_variant P326P 978G>T COAD-US 16 718514 718514 single base substitution C G downstream_gene_variant COAD-US 16 720960 720960 single base substitution C T downstream_gene_variant COAD-US 16 721703 721703 single base substitution C T downstream_gene_variant COAD-US 16 721872 721872 single base substitution G A downstream_gene_variant COAD-US 16 721964 721964 single base substitution C T downstream_gene_variant COAD-US 16 722331 722331 single base substitution C T downstream_gene_variant COAD-US 16 722548 722548 single base substitution A G downstream_gene_variant COCA-CN 16 697480 697480 single base substitution C A upstream_gene_variant COCA-CN 16 701098 701098 single base substitution C T exon_variant COCA-CN 16 701098 701098 single base substitution C T synonymous_variant H221H 663C>T COCA-CN 16 701098 701098 single base substitution C T upstream_gene_variant COCA-CN 16 701303 701303 single base substitution C T intron_variant COCA-CN 16 701303 701303 single base substitution C T upstream_gene_variant COCA-CN 16 701578 701578 single base substitution C T intron_variant COCA-CN 16 701578 701578 single base substitution C T upstream_gene_variant COCA-CN 16 701974 701974 single base substitution G A exon_variant COCA-CN 16 701974 701974 single base substitution G A missense_variant A330T 988G>A COCA-CN 16 701974 701974 single base substitution G A upstream_gene_variant COCA-CN 16 702408 702408 single base substitution C T exon_variant COCA-CN 16 702408 702408 single base substitution C T intron_variant COCA-CN 16 702408 702408 single base substitution C T upstream_gene_variant COCA-CN 16 702583 702583 single base substitution G A intron_variant COCA-CN 16 702583 702583 single base substitution G A upstream_gene_variant COCA-CN 16 705169 705169 single base substitution G A downstream_gene_variant COCA-CN 16 705169 705169 single base substitution G A exon_variant COCA-CN 16 705169 705169 single base substitution G A intron_variant COCA-CN 16 705169 705169 single base substitution G A upstream_gene_variant COCA-CN 16 708071 708071 single base substitution G C downstream_gene_variant COCA-CN 16 708071 708071 single base substitution G C intron_variant COCA-CN 16 708071 708071 single base substitution G C upstream_gene_variant COCA-CN 16 710211 710211 single base substitution C G downstream_gene_variant COCA-CN 16 710211 710211 single base substitution C G intron_variant COCA-CN 16 710211 710211 single base substitution C G upstream_gene_variant COCA-CN 16 712147 712147 single base substitution C T downstream_gene_variant COCA-CN 16 712147 712147 single base substitution C T intron_variant COCA-CN 16 712147 712147 single base substitution C T upstream_gene_variant COCA-CN 16 712499 712499 single base substitution C T downstream_gene_variant COCA-CN 16 712499 712499 single base substitution C T exon_variant COCA-CN 16 712499 712499 single base substitution C T intron_variant COCA-CN 16 712499 712499 single base substitution C T upstream_gene_variant COCA-CN 16 717650 717650 single base substitution G T 3_prime_UTR_variant COCA-CN 16 717650 717650 single base substitution G T downstream_gene_variant COCA-CN 16 717650 717650 single base substitution G T exon_variant COCA-CN 16 717650 717650 single base substitution G T missense_variant Q72H 216G>T COCA-CN 16 720071 720071 single base substitution G A downstream_gene_variant COCA-CN 16 720337 720337 single base substitution G A downstream_gene_variant COCA-CN 16 721120 721120 single base substitution C A downstream_gene_variant COCA-CN 16 721378 721378 single base substitution A C downstream_gene_variant COCA-CN 16 721403 721403 single base substitution A G downstream_gene_variant COCA-CN 16 721406 721406 single base substitution C G downstream_gene_variant COCA-CN 16 721413 721413 single base substitution T G downstream_gene_variant COCA-CN 16 721815 721815 single base substitution C T downstream_gene_variant COCA-CN 16 721983 721983 single base substitution G A downstream_gene_variant COCA-CN 16 722206 722206 single base substitution T C downstream_gene_variant ESAD-UK 16 695291 695291 single base substitution C G upstream_gene_variant ESAD-UK 16 696123 696123 single base substitution G C upstream_gene_variant ESAD-UK 16 696945 696945 single base substitution G A upstream_gene_variant ESAD-UK 16 697606 697606 single base substitution A G upstream_gene_variant ESAD-UK 16 698936 698936 single base substitution C T upstream_gene_variant ESAD-UK 16 700729 700729 single base substitution T A intron_variant ESAD-UK 16 700729 700729 single base substitution T A upstream_gene_variant ESAD-UK 16 701567 701567 single base substitution C T intron_variant ESAD-UK 16 701567 701567 single base substitution C T upstream_gene_variant ESAD-UK 16 702391 702391 single base substitution C T exon_variant ESAD-UK 16 702391 702391 single base substitution C T intron_variant ESAD-UK 16 702391 702391 single base substitution C T upstream_gene_variant ESAD-UK 16 705658 705658 single base substitution C T downstream_gene_variant ESAD-UK 16 705658 705658 single base substitution C T exon_variant ESAD-UK 16 705658 705658 single base substitution C T missense_variant R602W 1804C>T ESAD-UK 16 705658 705658 single base substitution C T upstream_gene_variant ESAD-UK 16 706178 706178 single base substitution C T downstream_gene_variant ESAD-UK 16 706178 706178 single base substitution C T exon_variant ESAD-UK 16 706178 706178 single base substitution C T intron_variant ESAD-UK 16 706178 706178 single base substitution C T upstream_gene_variant ESAD-UK 16 709271 709271 single base substitution G A downstream_gene_variant ESAD-UK 16 709271 709271 single base substitution G A exon_variant ESAD-UK 16 709271 709271 single base substitution G A missense_variant A1027T 3079G>A ESAD-UK 16 709271 709271 single base substitution G A missense_variant A9T 25G>A ESAD-UK 16 709271 709271 single base substitution G A upstream_gene_variant ESAD-UK 16 710332 710332 single base substitution C T downstream_gene_variant ESAD-UK 16 710332 710332 single base substitution C T intron_variant ESAD-UK 16 710332 710332 single base substitution C T upstream_gene_variant ESAD-UK 16 710706 710706 single base substitution C T downstream_gene_variant ESAD-UK 16 710706 710706 single base substitution C T exon_variant ESAD-UK 16 710706 710706 single base substitution C T missense_variant P1128L 3383C>T ESAD-UK 16 710706 710706 single base substitution C T missense_variant P130L 389C>T ESAD-UK 16 710706 710706 single base substitution C T upstream_gene_variant ESAD-UK 16 716065 716065 single base substitution T C 3_prime_UTR_variant ESAD-UK 16 716065 716065 single base substitution T C downstream_gene_variant ESAD-UK 16 716065 716065 single base substitution T C exon_variant ESAD-UK 16 716065 716065 single base substitution T C missense_variant M116T 347T>C ESAD-UK 16 716065 716065 single base substitution T C missense_variant M1517T 4550T>C ESAD-UK 16 716065 716065 single base substitution T C missense_variant M1519T 4556T>C ESAD-UK 16 716065 716065 single base substitution T C upstream_gene_variant ESAD-UK 16 716929 716929 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 16 716929 716929 deletion of <=200bp T - downstream_gene_variant ESAD-UK 16 716929 716929 deletion of <=200bp T - exon_variant ESAD-UK 16 716929 716929 deletion of <=200bp T - frameshift_variant F1677 ESAD-UK 16 716929 716929 deletion of <=200bp T - frameshift_variant F1679 ESAD-UK 16 716929 716929 deletion of <=200bp T - frameshift_variant F228 ESAD-UK 16 716929 716929 deletion of <=200bp T - frameshift_variant F276 ESAD-UK 16 716929 716929 deletion of <=200bp T - frameshift_variant F7 ESAD-UK 16 716929 716929 deletion of <=200bp T - intron_variant ESAD-UK 16 717037 717037 single base substitution G T downstream_gene_variant ESAD-UK 16 717037 717037 single base substitution G T intron_variant ESAD-UK 16 717095 717095 single base substitution G A downstream_gene_variant ESAD-UK 16 717095 717095 single base substitution G A intron_variant ESAD-UK 16 718893 718893 single base substitution C T downstream_gene_variant ESAD-UK 16 719854 719854 single base substitution G C downstream_gene_variant ESAD-UK 16 722527 722527 single base substitution C T downstream_gene_variant ESAD-UK 16 722760 722760 single base substitution G A downstream_gene_variant ESCA-CN 16 697988 697989 deletion of <=200bp TT - upstream_gene_variant ESCA-CN 16 702507 702507 single base substitution T A exon_variant ESCA-CN 16 702507 702507 single base substitution T A missense_variant I365N 1094T>A ESCA-CN 16 702507 702507 single base substitution T A upstream_gene_variant ESCA-CN 16 705424 705424 single base substitution C G downstream_gene_variant ESCA-CN 16 705424 705424 single base substitution C G exon_variant ESCA-CN 16 705424 705424 single base substitution C G missense_variant F558L 1674C>G ESCA-CN 16 705424 705424 single base substitution C G upstream_gene_variant ESCA-CN 16 705795 705795 single base substitution C T downstream_gene_variant ESCA-CN 16 705795 705795 single base substitution C T exon_variant ESCA-CN 16 705795 705795 single base substitution C T synonymous_variant S624S 1872C>T ESCA-CN 16 705795 705795 single base substitution C T upstream_gene_variant ESCA-CN 16 709367 709367 single base substitution G C downstream_gene_variant ESCA-CN 16 709367 709367 single base substitution G C exon_variant ESCA-CN 16 709367 709367 single base substitution G C missense_variant G1059R 3175G>C ESCA-CN 16 709367 709367 single base substitution G C missense_variant G41R 121G>C ESCA-CN 16 709367 709367 single base substitution G C upstream_gene_variant ESCA-CN 16 710808 710808 single base substitution G A downstream_gene_variant ESCA-CN 16 710808 710808 single base substitution G A exon_variant ESCA-CN 16 710808 710808 single base substitution G A intron_variant ESCA-CN 16 710808 710808 single base substitution G A upstream_gene_variant ESCA-CN 16 711750 711750 single base substitution G T 3_prime_UTR_variant ESCA-CN 16 711750 711750 single base substitution G T downstream_gene_variant ESCA-CN 16 711750 711750 single base substitution G T exon_variant ESCA-CN 16 711750 711750 single base substitution G T missense_variant W1276L 3827G>T ESCA-CN 16 711750 711750 single base substitution G T upstream_gene_variant ESCA-CN 16 718366 718366 single base substitution G C downstream_gene_variant GBM-US 16 701986 701986 single base substitution G A exon_variant GBM-US 16 701986 701986 single base substitution G A missense_variant V334M 1000G>A GBM-US 16 701986 701986 single base substitution G A upstream_gene_variant GBM-US 16 703407 703407 single base substitution G A exon_variant GBM-US 16 703407 703407 single base substitution G A missense_variant V397M 1189G>A GBM-US 16 703407 703407 single base substitution G A upstream_gene_variant GBM-US 16 703568 703568 single base substitution C T downstream_gene_variant GBM-US 16 703568 703568 single base substitution C T exon_variant GBM-US 16 703568 703568 single base substitution C T missense_variant S426L 1277C>T GBM-US 16 703568 703568 single base substitution C T upstream_gene_variant GBM-US 16 703624 703624 single base substitution T G downstream_gene_variant GBM-US 16 703624 703624 single base substitution T G exon_variant GBM-US 16 703624 703624 single base substitution T G missense_variant C445G 1333T>G GBM-US 16 703624 703624 single base substitution T G upstream_gene_variant GBM-US 16 715745 715745 single base substitution C T 3_prime_UTR_variant GBM-US 16 715745 715745 single base substitution C T downstream_gene_variant GBM-US 16 715745 715745 single base substitution C T exon_variant GBM-US 16 715745 715745 single base substitution C T missense_variant R1460W 4378C>T GBM-US 16 715745 715745 single base substitution C T missense_variant R1462W 4384C>T GBM-US 16 715745 715745 single base substitution C T missense_variant R59W 175C>T GBM-US 16 715745 715745 single base substitution C T upstream_gene_variant KIRC-US 16 720301 720301 single base substitution A G downstream_gene_variant KIRC-US 16 720318 720318 single base substitution C T downstream_gene_variant KIRC-US 16 720686 720686 single base substitution G A downstream_gene_variant KIRC-US 16 722787 722787 single base substitution G A downstream_gene_variant KIRP-US 16 707223 707223 single base substitution T G downstream_gene_variant KIRP-US 16 707223 707223 single base substitution T G exon_variant KIRP-US 16 707223 707223 single base substitution T G splice_donor_variant KIRP-US 16 707223 707223 single base substitution T G upstream_gene_variant KIRP-US 16 707787 707787 single base substitution C T downstream_gene_variant KIRP-US 16 707787 707787 single base substitution C T exon_variant KIRP-US 16 707787 707787 single base substitution C T synonymous_variant P833P 2499C>T KIRP-US 16 707787 707787 single base substitution C T upstream_gene_variant KIRP-US 16 716291 716291 single base substitution C A 3_prime_UTR_variant KIRP-US 16 716291 716291 single base substitution C A downstream_gene_variant KIRP-US 16 716291 716291 single base substitution C A exon_variant KIRP-US 16 716291 716291 single base substitution C A missense_variant R1561S 4681C>A KIRP-US 16 716291 716291 single base substitution C A missense_variant R1563S 4687C>A KIRP-US 16 716291 716291 single base substitution C A missense_variant R160S 478C>A KIRP-US 16 716291 716291 single base substitution C A upstream_gene_variant LAML-KR 16 701296 701296 single base substitution G C intron_variant LAML-KR 16 701296 701296 single base substitution G C upstream_gene_variant LAML-KR 16 701656 701656 single base substitution C T exon_variant LAML-KR 16 701656 701656 single base substitution C T missense_variant P250L 749C>T LAML-KR 16 701656 701656 single base substitution C T upstream_gene_variant LAML-KR 16 705254 705254 single base substitution G T downstream_gene_variant LAML-KR 16 705254 705254 single base substitution G T exon_variant LAML-KR 16 705254 705254 single base substitution G T intron_variant LAML-KR 16 705254 705254 single base substitution G T upstream_gene_variant LAML-KR 16 711524 711524 single base substitution G A downstream_gene_variant LAML-KR 16 711524 711524 single base substitution G A intron_variant LAML-KR 16 711524 711524 single base substitution G A upstream_gene_variant LAML-KR 16 715325 715325 single base substitution C T 5_prime_UTR_variant LAML-KR 16 715325 715325 single base substitution C T downstream_gene_variant LAML-KR 16 715325 715325 single base substitution C T exon_variant LAML-KR 16 715325 715325 single base substitution C T intron_variant LAML-KR 16 715325 715325 single base substitution C T upstream_gene_variant LAML-KR 16 721815 721815 single base substitution C T downstream_gene_variant LGG-US 16 709106 709106 deletion of <=200bp C - downstream_gene_variant LGG-US 16 709106 709106 deletion of <=200bp C - exon_variant LGG-US 16 709106 709106 deletion of <=200bp C - frameshift_variant A1011 LGG-US 16 709106 709106 deletion of <=200bp C - upstream_gene_variant LICA-CN 16 719599 719599 single base substitution T C downstream_gene_variant LICA-FR 16 703648 703648 single base substitution A T downstream_gene_variant LICA-FR 16 703648 703648 single base substitution A T exon_variant LICA-FR 16 703648 703648 single base substitution A T missense_variant M453L 1357A>T LICA-FR 16 703648 703648 single base substitution A T upstream_gene_variant LICA-FR 16 705038 705038 single base substitution G A downstream_gene_variant LICA-FR 16 705038 705038 single base substitution G A exon_variant LICA-FR 16 705038 705038 single base substitution G A missense_variant A483T 1447G>A LICA-FR 16 705038 705038 single base substitution G A upstream_gene_variant LICA-FR 16 707817 707817 single base substitution G A downstream_gene_variant LICA-FR 16 707817 707817 single base substitution G A exon_variant LICA-FR 16 707817 707817 single base substitution G A synonymous_variant R843R 2529G>A LICA-FR 16 707817 707817 single base substitution G A upstream_gene_variant LICA-FR 16 711737 711737 single base substitution A C 3_prime_UTR_variant LICA-FR 16 711737 711737 single base substitution A C downstream_gene_variant LICA-FR 16 711737 711737 single base substitution A C exon_variant LICA-FR 16 711737 711737 single base substitution A C missense_variant T1272P 3814A>C LICA-FR 16 711737 711737 single base substitution A C upstream_gene_variant LICA-FR 16 712781 712781 single base substitution G T downstream_gene_variant LICA-FR 16 712781 712781 single base substitution G T exon_variant LICA-FR 16 712781 712781 single base substitution G T intron_variant LICA-FR 16 712781 712781 single base substitution G T synonymous_variant T1416T 4248G>T LICA-FR 16 712781 712781 single base substitution G T synonymous_variant T1418T 4254G>T LICA-FR 16 712781 712781 single base substitution G T upstream_gene_variant LICA-FR 16 716067 716067 single base substitution G A 3_prime_UTR_variant LICA-FR 16 716067 716067 single base substitution G A downstream_gene_variant LICA-FR 16 716067 716067 single base substitution G A exon_variant LICA-FR 16 716067 716067 single base substitution G A missense_variant E117K 349G>A LICA-FR 16 716067 716067 single base substitution G A missense_variant E1518K 4552G>A LICA-FR 16 716067 716067 single base substitution G A missense_variant E1520K 4558G>A LICA-FR 16 716067 716067 single base substitution G A upstream_gene_variant LIHC-US 16 699822 699822 single base substitution T C exon_variant LIHC-US 16 699822 699822 single base substitution T C missense_variant S24P 70T>C LIHC-US 16 699822 699822 single base substitution T C upstream_gene_variant LIHC-US 16 709346 709346 single base substitution G A downstream_gene_variant LIHC-US 16 709346 709346 single base substitution G A exon_variant LIHC-US 16 709346 709346 single base substitution G A missense_variant V1052I 3154G>A LIHC-US 16 709346 709346 single base substitution G A missense_variant V34I 100G>A LIHC-US 16 709346 709346 single base substitution G A upstream_gene_variant LIHC-US 16 712780 712780 single base substitution C T downstream_gene_variant LIHC-US 16 712780 712780 single base substitution C T exon_variant LIHC-US 16 712780 712780 single base substitution C T intron_variant LIHC-US 16 712780 712780 single base substitution C T missense_variant T1416M 4247C>T LIHC-US 16 712780 712780 single base substitution C T missense_variant T1418M 4253C>T LIHC-US 16 712780 712780 single base substitution C T upstream_gene_variant LINC-JP 16 695730 695730 single base substitution C G upstream_gene_variant LINC-JP 16 696536 696536 single base substitution G A upstream_gene_variant LINC-JP 16 697909 697909 single base substitution C A upstream_gene_variant LINC-JP 16 698153 698153 single base substitution C T upstream_gene_variant LINC-JP 16 699976 699976 single base substitution C A intron_variant LINC-JP 16 699976 699976 single base substitution C A upstream_gene_variant LINC-JP 16 701459 701459 single base substitution G A intron_variant LINC-JP 16 701459 701459 single base substitution G A upstream_gene_variant LINC-JP 16 701965 701965 single base substitution A T exon_variant LINC-JP 16 701965 701965 single base substitution A T missense_variant T327S 979A>T LINC-JP 16 701965 701965 single base substitution A T upstream_gene_variant LINC-JP 16 709179 709179 deletion of <=200bp G - downstream_gene_variant LINC-JP 16 709179 709179 deletion of <=200bp G - intron_variant LINC-JP 16 709179 709179 deletion of <=200bp G - upstream_gene_variant LINC-JP 16 711311 711311 single base substitution C T downstream_gene_variant LINC-JP 16 711311 711311 single base substitution C T exon_variant LINC-JP 16 711311 711311 single base substitution C T intron_variant LINC-JP 16 711311 711311 single base substitution C T upstream_gene_variant LINC-JP 16 720683 720683 single base substitution C T downstream_gene_variant LINC-JP 16 722298 722298 single base substitution C T downstream_gene_variant LIRI-JP 16 695831 695831 single base substitution C A upstream_gene_variant LIRI-JP 16 695887 695887 insertion of <=200bp - T upstream_gene_variant LIRI-JP 16 696005 696005 single base substitution G A upstream_gene_variant LIRI-JP 16 697152 697152 insertion of <=200bp - T upstream_gene_variant LIRI-JP 16 697405 697405 single base substitution C A upstream_gene_variant LIRI-JP 16 700547 700547 single base substitution G A exon_variant LIRI-JP 16 700547 700547 single base substitution G A missense_variant G133S 397G>A LIRI-JP 16 700547 700547 single base substitution G A upstream_gene_variant LIRI-JP 16 702200 702200 single base substitution G T exon_variant LIRI-JP 16 702200 702200 single base substitution G T intron_variant LIRI-JP 16 702200 702200 single base substitution G T upstream_gene_variant LIRI-JP 16 703265 703265 single base substitution G A intron_variant LIRI-JP 16 703265 703265 single base substitution G A upstream_gene_variant LIRI-JP 16 708882 708882 single base substitution G A downstream_gene_variant LIRI-JP 16 708882 708882 single base substitution G A intron_variant LIRI-JP 16 708882 708882 single base substitution G A upstream_gene_variant LUSC-KR 16 701395 701395 single base substitution G A intron_variant LUSC-KR 16 701395 701395 single base substitution G A upstream_gene_variant LUSC-KR 16 701795 701795 single base substitution C A intron_variant LUSC-KR 16 701795 701795 single base substitution C A upstream_gene_variant LUSC-KR 16 706769 706769 single base substitution C T downstream_gene_variant LUSC-KR 16 706769 706769 single base substitution C T exon_variant LUSC-KR 16 706769 706769 single base substitution C T intron_variant LUSC-KR 16 706769 706769 single base substitution C T missense_variant A747V 2240C>T LUSC-KR 16 706769 706769 single base substitution C T upstream_gene_variant LUSC-KR 16 715325 715325 single base substitution C T 5_prime_UTR_variant LUSC-KR 16 715325 715325 single base substitution C T downstream_gene_variant LUSC-KR 16 715325 715325 single base substitution C T exon_variant LUSC-KR 16 715325 715325 single base substitution C T intron_variant LUSC-KR 16 715325 715325 single base substitution C T upstream_gene_variant LUSC-KR 16 717135 717135 single base substitution C A downstream_gene_variant LUSC-KR 16 717135 717135 single base substitution C A intron_variant LUSC-KR 16 718094 718094 single base substitution G A downstream_gene_variant LUSC-KR 16 719496 719496 single base substitution G A downstream_gene_variant LUSC-KR 16 721087 721087 single base substitution C T downstream_gene_variant LUSC-US 16 703577 703577 single base substitution C A downstream_gene_variant LUSC-US 16 703577 703577 single base substitution C A exon_variant LUSC-US 16 703577 703577 single base substitution C A missense_variant A429E 1286C>A LUSC-US 16 703577 703577 single base substitution C A upstream_gene_variant LUSC-US 16 705883 705883 single base substitution G A downstream_gene_variant LUSC-US 16 705883 705883 single base substitution G A exon_variant LUSC-US 16 705883 705883 single base substitution G A missense_variant E654K 1960G>A LUSC-US 16 705883 705883 single base substitution G A splice_region_variant LUSC-US 16 705883 705883 single base substitution G A upstream_gene_variant LUSC-US 16 708258 708258 single base substitution C T downstream_gene_variant LUSC-US 16 708258 708258 single base substitution C T exon_variant LUSC-US 16 708258 708258 single base substitution C T missense_variant P894S 2680C>T LUSC-US 16 708258 708258 single base substitution C T upstream_gene_variant LUSC-US 16 708597 708597 single base substitution G T downstream_gene_variant LUSC-US 16 708597 708597 single base substitution G T exon_variant LUSC-US 16 708597 708597 single base substitution G T missense_variant A947S 2839G>T LUSC-US 16 708597 708597 single base substitution G T upstream_gene_variant LUSC-US 16 711941 711941 single base substitution G C 3_prime_UTR_variant LUSC-US 16 711941 711941 single base substitution G C downstream_gene_variant LUSC-US 16 711941 711941 single base substitution G C exon_variant LUSC-US 16 711941 711941 single base substitution G C synonymous_variant S1305S 3915G>C LUSC-US 16 711941 711941 single base substitution G C upstream_gene_variant LUSC-US 16 712030 712030 single base substitution T C 3_prime_UTR_variant LUSC-US 16 712030 712030 single base substitution T C downstream_gene_variant LUSC-US 16 712030 712030 single base substitution T C exon_variant LUSC-US 16 712030 712030 single base substitution T C missense_variant L1335S 4004T>C LUSC-US 16 712030 712030 single base substitution T C upstream_gene_variant LUSC-US 16 716485 716485 single base substitution C G 3_prime_UTR_variant LUSC-US 16 716485 716485 single base substitution C G downstream_gene_variant LUSC-US 16 716485 716485 single base substitution C G exon_variant LUSC-US 16 716485 716485 single base substitution C G intron_variant LUSC-US 16 716485 716485 single base substitution C G missense_variant L1591V 4771C>G LUSC-US 16 716485 716485 single base substitution C G missense_variant L1593V 4777C>G LUSC-US 16 716485 716485 single base substitution C G missense_variant L190V 568C>G LUSC-US 16 716485 716485 single base substitution C G upstream_gene_variant LUSC-US 16 722740 722740 single base substitution C T downstream_gene_variant MALY-DE 16 696978 696978 single base substitution G A upstream_gene_variant MALY-DE 16 697184 697184 single base substitution C G upstream_gene_variant MALY-DE 16 698243 698243 single base substitution G A upstream_gene_variant MALY-DE 16 698323 698323 single base substitution T C upstream_gene_variant MALY-DE 16 705001 705001 single base substitution G A downstream_gene_variant MALY-DE 16 705001 705001 single base substitution G A exon_variant MALY-DE 16 705001 705001 single base substitution G A intron_variant MALY-DE 16 705001 705001 single base substitution G A upstream_gene_variant MALY-DE 16 711539 711539 single base substitution A T downstream_gene_variant MALY-DE 16 711539 711539 single base substitution A T intron_variant MALY-DE 16 711539 711539 single base substitution A T upstream_gene_variant MALY-DE 16 716806 716806 single base substitution C G downstream_gene_variant MALY-DE 16 716806 716806 single base substitution C G intron_variant MALY-DE 16 716806 716806 single base substitution C G upstream_gene_variant MALY-DE 16 721351 721351 single base substitution T C downstream_gene_variant MELA-AU 16 695010 695010 single base substitution G A upstream_gene_variant MELA-AU 16 695663 695663 single base substitution C T upstream_gene_variant MELA-AU 16 696007 696007 single base substitution G A upstream_gene_variant MELA-AU 16 696383 696383 single base substitution C T upstream_gene_variant MELA-AU 16 696447 696447 single base substitution C T upstream_gene_variant MELA-AU 16 696672 696672 single base substitution G A upstream_gene_variant MELA-AU 16 696705 696705 single base substitution C T upstream_gene_variant MELA-AU 16 696925 696925 single base substitution C T upstream_gene_variant MELA-AU 16 697544 697544 single base substitution G A upstream_gene_variant MELA-AU 16 699264 699265 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 699549 699549 single base substitution G A exon_variant MELA-AU 16 699549 699549 single base substitution G A intron_variant MELA-AU 16 699549 699549 single base substitution G A upstream_gene_variant MELA-AU 16 699889 699890 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 699889 699890 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 700053 700053 single base substitution C T exon_variant MELA-AU 16 700053 700053 single base substitution C T synonymous_variant I55I 165C>T MELA-AU 16 700053 700053 single base substitution C T upstream_gene_variant MELA-AU 16 700227 700227 single base substitution C T intron_variant MELA-AU 16 700227 700227 single base substitution C T upstream_gene_variant MELA-AU 16 700959 700959 single base substitution G A intron_variant MELA-AU 16 700959 700959 single base substitution G A upstream_gene_variant MELA-AU 16 701056 701056 single base substitution C T exon_variant MELA-AU 16 701056 701056 single base substitution C T synonymous_variant F207F 621C>T MELA-AU 16 701056 701056 single base substitution C T upstream_gene_variant MELA-AU 16 701390 701390 single base substitution G A intron_variant MELA-AU 16 701390 701390 single base substitution G A upstream_gene_variant MELA-AU 16 702472 702473 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 16 702472 702473 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant FL353FF MELA-AU 16 702472 702473 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 702664 702664 single base substitution C T intron_variant MELA-AU 16 702664 702664 single base substitution C T upstream_gene_variant MELA-AU 16 702679 702679 single base substitution C T intron_variant MELA-AU 16 702679 702679 single base substitution C T upstream_gene_variant MELA-AU 16 703020 703020 single base substitution C T intron_variant MELA-AU 16 703020 703020 single base substitution C T upstream_gene_variant MELA-AU 16 703330 703330 single base substitution C T intron_variant MELA-AU 16 703330 703330 single base substitution C T upstream_gene_variant MELA-AU 16 703956 703956 single base substitution C T downstream_gene_variant MELA-AU 16 703956 703956 single base substitution C T exon_variant MELA-AU 16 703956 703956 single base substitution C T intron_variant MELA-AU 16 703956 703956 single base substitution C T upstream_gene_variant MELA-AU 16 704318 704318 single base substitution C T downstream_gene_variant MELA-AU 16 704318 704318 single base substitution C T exon_variant MELA-AU 16 704318 704318 single base substitution C T intron_variant MELA-AU 16 704318 704318 single base substitution C T upstream_gene_variant MELA-AU 16 705091 705092 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 705091 705092 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 16 705091 705092 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant KA500KT MELA-AU 16 705091 705092 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 705220 705220 single base substitution C T downstream_gene_variant MELA-AU 16 705220 705220 single base substitution C T exon_variant MELA-AU 16 705220 705220 single base substitution C T intron_variant MELA-AU 16 705220 705220 single base substitution C T upstream_gene_variant MELA-AU 16 705222 705222 single base substitution C T downstream_gene_variant MELA-AU 16 705222 705222 single base substitution C T exon_variant MELA-AU 16 705222 705222 single base substitution C T intron_variant MELA-AU 16 705222 705222 single base substitution C T upstream_gene_variant MELA-AU 16 705376 705376 single base substitution C T downstream_gene_variant MELA-AU 16 705376 705376 single base substitution C T exon_variant MELA-AU 16 705376 705376 single base substitution C T synonymous_variant P542P 1626C>T MELA-AU 16 705376 705376 single base substitution C T upstream_gene_variant MELA-AU 16 705761 705761 single base substitution C T downstream_gene_variant MELA-AU 16 705761 705761 single base substitution C T intron_variant MELA-AU 16 705761 705761 single base substitution C T upstream_gene_variant MELA-AU 16 706087 706088 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 706087 706088 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 16 706087 706088 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 706087 706088 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 706349 706349 single base substitution C T downstream_gene_variant MELA-AU 16 706349 706349 single base substitution C T exon_variant MELA-AU 16 706349 706349 single base substitution C T missense_variant R672C 2014C>T MELA-AU 16 706349 706349 single base substitution C T upstream_gene_variant MELA-AU 16 706424 706424 single base substitution C T downstream_gene_variant MELA-AU 16 706424 706424 single base substitution C T exon_variant MELA-AU 16 706424 706424 single base substitution C T missense_variant R697C 2089C>T MELA-AU 16 706424 706424 single base substitution C T upstream_gene_variant MELA-AU 16 706989 706989 single base substitution C T downstream_gene_variant MELA-AU 16 706989 706989 single base substitution C T intron_variant MELA-AU 16 706989 706989 single base substitution C T upstream_gene_variant MELA-AU 16 707196 707196 single base substitution C T downstream_gene_variant MELA-AU 16 707196 707196 single base substitution C T exon_variant MELA-AU 16 707196 707196 single base substitution C T synonymous_variant P816P 2448C>T MELA-AU 16 707196 707196 single base substitution C T upstream_gene_variant MELA-AU 16 707314 707315 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 707314 707315 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 16 707314 707315 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 707314 707315 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 707733 707733 single base substitution C T downstream_gene_variant MELA-AU 16 707733 707733 single base substitution C T intron_variant MELA-AU 16 707733 707733 single base substitution C T upstream_gene_variant MELA-AU 16 707794 707794 single base substitution C T downstream_gene_variant MELA-AU 16 707794 707794 single base substitution C T exon_variant MELA-AU 16 707794 707794 single base substitution C T missense_variant P836S 2506C>T MELA-AU 16 707794 707794 single base substitution C T upstream_gene_variant MELA-AU 16 708121 708122 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 708121 708122 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 708121 708122 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 708383 708383 single base substitution C T downstream_gene_variant MELA-AU 16 708383 708383 single base substitution C T intron_variant MELA-AU 16 708383 708383 single base substitution C T upstream_gene_variant MELA-AU 16 708782 708782 single base substitution C T downstream_gene_variant MELA-AU 16 708782 708782 single base substitution C T intron_variant MELA-AU 16 708782 708782 single base substitution C T upstream_gene_variant MELA-AU 16 709294 709294 single base substitution C T downstream_gene_variant MELA-AU 16 709294 709294 single base substitution C T exon_variant MELA-AU 16 709294 709294 single base substitution C T synonymous_variant L1034L 3102C>T MELA-AU 16 709294 709294 single base substitution C T synonymous_variant L16L 48C>T MELA-AU 16 709294 709294 single base substitution C T upstream_gene_variant MELA-AU 16 709625 709625 single base substitution C T downstream_gene_variant MELA-AU 16 709625 709625 single base substitution C T intron_variant MELA-AU 16 709625 709625 single base substitution C T upstream_gene_variant MELA-AU 16 710293 710294 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 710293 710294 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 710293 710294 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 710312 710312 single base substitution C T downstream_gene_variant MELA-AU 16 710312 710312 single base substitution C T intron_variant MELA-AU 16 710312 710312 single base substitution C T upstream_gene_variant MELA-AU 16 710441 710441 single base substitution C T downstream_gene_variant MELA-AU 16 710441 710441 single base substitution C T intron_variant MELA-AU 16 710441 710441 single base substitution C T upstream_gene_variant MELA-AU 16 711227 711227 single base substitution C T downstream_gene_variant MELA-AU 16 711227 711227 single base substitution C T exon_variant MELA-AU 16 711227 711227 single base substitution C T intron_variant MELA-AU 16 711227 711227 single base substitution C T upstream_gene_variant MELA-AU 16 711475 711475 single base substitution C T 3_prime_UTR_variant MELA-AU 16 711475 711475 single base substitution C T downstream_gene_variant MELA-AU 16 711475 711475 single base substitution C T exon_variant MELA-AU 16 711475 711475 single base substitution C T missense_variant P1216L 3647C>T MELA-AU 16 711475 711475 single base substitution C T upstream_gene_variant MELA-AU 16 711544 711544 single base substitution C T downstream_gene_variant MELA-AU 16 711544 711544 single base substitution C T intron_variant MELA-AU 16 711544 711544 single base substitution C T upstream_gene_variant MELA-AU 16 711669 711669 single base substitution C T 3_prime_UTR_variant MELA-AU 16 711669 711669 single base substitution C T downstream_gene_variant MELA-AU 16 711669 711669 single base substitution C T exon_variant MELA-AU 16 711669 711669 single base substitution C T missense_variant P1249L 3746C>T MELA-AU 16 711669 711669 single base substitution C T upstream_gene_variant MELA-AU 16 711731 711731 single base substitution C A 3_prime_UTR_variant MELA-AU 16 711731 711731 single base substitution C A downstream_gene_variant MELA-AU 16 711731 711731 single base substitution C A exon_variant MELA-AU 16 711731 711731 single base substitution C A missense_variant Q1270K 3808C>A MELA-AU 16 711731 711731 single base substitution C A upstream_gene_variant MELA-AU 16 712740 712740 single base substitution G T downstream_gene_variant MELA-AU 16 712740 712740 single base substitution G T exon_variant MELA-AU 16 712740 712740 single base substitution G T intron_variant MELA-AU 16 712740 712740 single base substitution G T missense_variant D1403Y 4207G>T MELA-AU 16 712740 712740 single base substitution G T missense_variant D1405Y 4213G>T MELA-AU 16 712740 712740 single base substitution G T upstream_gene_variant MELA-AU 16 712966 712966 single base substitution C T downstream_gene_variant MELA-AU 16 712966 712966 single base substitution C T exon_variant MELA-AU 16 712966 712966 single base substitution C T intron_variant MELA-AU 16 712966 712966 single base substitution C T upstream_gene_variant MELA-AU 16 713017 713017 single base substitution C T downstream_gene_variant MELA-AU 16 713017 713017 single base substitution C T exon_variant MELA-AU 16 713017 713017 single base substitution C T intron_variant MELA-AU 16 713017 713017 single base substitution C T upstream_gene_variant MELA-AU 16 713321 713321 single base substitution C T downstream_gene_variant MELA-AU 16 713321 713321 single base substitution C T exon_variant MELA-AU 16 713321 713321 single base substitution C T intron_variant MELA-AU 16 713321 713321 single base substitution C T upstream_gene_variant MELA-AU 16 713517 713517 single base substitution G A downstream_gene_variant MELA-AU 16 713517 713517 single base substitution G A exon_variant MELA-AU 16 713517 713517 single base substitution G A intron_variant MELA-AU 16 713517 713517 single base substitution G A upstream_gene_variant MELA-AU 16 713711 713711 single base substitution C T downstream_gene_variant MELA-AU 16 713711 713711 single base substitution C T intron_variant MELA-AU 16 713711 713711 single base substitution C T upstream_gene_variant MELA-AU 16 713842 713842 single base substitution C T downstream_gene_variant MELA-AU 16 713842 713842 single base substitution C T intron_variant MELA-AU 16 713842 713842 single base substitution C T upstream_gene_variant MELA-AU 16 713903 713903 single base substitution C T downstream_gene_variant MELA-AU 16 713903 713903 single base substitution C T intron_variant MELA-AU 16 713903 713903 single base substitution C T upstream_gene_variant MELA-AU 16 713958 713958 single base substitution T A downstream_gene_variant MELA-AU 16 713958 713958 single base substitution T A intron_variant MELA-AU 16 713958 713958 single base substitution T A upstream_gene_variant MELA-AU 16 713960 713960 single base substitution C T downstream_gene_variant MELA-AU 16 713960 713960 single base substitution C T intron_variant MELA-AU 16 713960 713960 single base substitution C T upstream_gene_variant MELA-AU 16 714115 714115 single base substitution C T downstream_gene_variant MELA-AU 16 714115 714115 single base substitution C T intron_variant MELA-AU 16 714115 714115 single base substitution C T upstream_gene_variant MELA-AU 16 714231 714231 single base substitution C T downstream_gene_variant MELA-AU 16 714231 714231 single base substitution C T intron_variant MELA-AU 16 714231 714231 single base substitution C T upstream_gene_variant MELA-AU 16 714533 714533 single base substitution T A downstream_gene_variant MELA-AU 16 714533 714533 single base substitution T A intron_variant MELA-AU 16 714533 714533 single base substitution T A upstream_gene_variant MELA-AU 16 714815 714815 single base substitution G A downstream_gene_variant MELA-AU 16 714815 714815 single base substitution G A intron_variant MELA-AU 16 714815 714815 single base substitution G A upstream_gene_variant MELA-AU 16 714913 714914 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 714913 714914 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 714913 714914 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 714995 714996 multiple base substitution (>=2bp and <=200bp) AA TT downstream_gene_variant MELA-AU 16 714995 714996 multiple base substitution (>=2bp and <=200bp) AA TT exon_variant MELA-AU 16 714995 714996 multiple base substitution (>=2bp and <=200bp) AA TT intron_variant MELA-AU 16 714995 714996 multiple base substitution (>=2bp and <=200bp) AA TT upstream_gene_variant MELA-AU 16 715013 715013 single base substitution C T downstream_gene_variant MELA-AU 16 715013 715013 single base substitution C T exon_variant MELA-AU 16 715013 715013 single base substitution C T intron_variant MELA-AU 16 715013 715013 single base substitution C T upstream_gene_variant MELA-AU 16 715151 715151 single base substitution C T downstream_gene_variant MELA-AU 16 715151 715151 single base substitution C T exon_variant MELA-AU 16 715151 715151 single base substitution C T intron_variant MELA-AU 16 715151 715151 single base substitution C T upstream_gene_variant MELA-AU 16 715539 715539 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 16 715539 715539 single base substitution C T downstream_gene_variant MELA-AU 16 715539 715539 single base substitution C T exon_variant MELA-AU 16 715539 715539 single base substitution C T intron_variant MELA-AU 16 715539 715539 single base substitution C T upstream_gene_variant MELA-AU 16 715651 715651 single base substitution C T downstream_gene_variant MELA-AU 16 715651 715651 single base substitution C T exon_variant MELA-AU 16 715651 715651 single base substitution C T intron_variant MELA-AU 16 715651 715651 single base substitution C T synonymous_variant H27H 81C>T MELA-AU 16 715651 715651 single base substitution C T upstream_gene_variant MELA-AU 16 716417 716417 single base substitution A T downstream_gene_variant MELA-AU 16 716417 716417 single base substitution A T intron_variant MELA-AU 16 716417 716417 single base substitution A T upstream_gene_variant MELA-AU 16 716808 716808 single base substitution C T downstream_gene_variant MELA-AU 16 716808 716808 single base substitution C T intron_variant MELA-AU 16 716808 716808 single base substitution C T upstream_gene_variant MELA-AU 16 716825 716825 single base substitution C T downstream_gene_variant MELA-AU 16 716825 716825 single base substitution C T intron_variant MELA-AU 16 716825 716825 single base substitution C T upstream_gene_variant MELA-AU 16 716970 716970 single base substitution C T 3_prime_UTR_variant MELA-AU 16 716970 716970 single base substitution C T downstream_gene_variant MELA-AU 16 716970 716970 single base substitution C T exon_variant MELA-AU 16 716970 716970 single base substitution C T intron_variant MELA-AU 16 716970 716970 single base substitution C T synonymous_variant L1690L 5070C>T MELA-AU 16 716970 716970 single base substitution C T synonymous_variant L1692L 5076C>T MELA-AU 16 716970 716970 single base substitution C T synonymous_variant L20L 60C>T MELA-AU 16 716970 716970 single base substitution C T synonymous_variant L241L 723C>T MELA-AU 16 716970 716970 single base substitution C T synonymous_variant L289L 867C>T MELA-AU 16 717714 717714 single base substitution C T 3_prime_UTR_variant MELA-AU 16 717714 717714 single base substitution C T downstream_gene_variant MELA-AU 16 717714 717714 single base substitution C T exon_variant MELA-AU 16 717714 717714 single base substitution C T missense_variant R94C 280C>T MELA-AU 16 718076 718076 single base substitution G A downstream_gene_variant MELA-AU 16 718102 718102 single base substitution G A downstream_gene_variant MELA-AU 16 719102 719102 single base substitution C T downstream_gene_variant MELA-AU 16 720261 720262 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 720460 720460 single base substitution C T downstream_gene_variant MELA-AU 16 720536 720536 single base substitution C T downstream_gene_variant MELA-AU 16 720590 720590 single base substitution C T downstream_gene_variant MELA-AU 16 720966 720966 single base substitution G A downstream_gene_variant MELA-AU 16 721259 721259 single base substitution C G downstream_gene_variant MELA-AU 16 721357 721357 single base substitution C T downstream_gene_variant MELA-AU 16 721510 721510 single base substitution C T downstream_gene_variant MELA-AU 16 721690 721690 single base substitution C T downstream_gene_variant MELA-AU 16 722045 722045 single base substitution C T downstream_gene_variant MELA-AU 16 722229 722229 single base substitution C T downstream_gene_variant MELA-AU 16 722354 722354 single base substitution C T downstream_gene_variant MELA-AU 16 722486 722486 single base substitution C T downstream_gene_variant MELA-AU 16 722680 722680 single base substitution C T downstream_gene_variant ORCA-IN 16 698128 698128 single base substitution C T upstream_gene_variant ORCA-IN 16 701493 701493 single base substitution C T intron_variant ORCA-IN 16 701493 701493 single base substitution C T upstream_gene_variant ORCA-IN 16 708641 708641 single base substitution C A downstream_gene_variant ORCA-IN 16 708641 708641 single base substitution C A exon_variant ORCA-IN 16 708641 708641 single base substitution C A intron_variant ORCA-IN 16 708641 708641 single base substitution C A missense_variant S961R 2883C>A ORCA-IN 16 708641 708641 single base substitution C A upstream_gene_variant ORCA-IN 16 711137 711137 single base substitution G A downstream_gene_variant ORCA-IN 16 711137 711137 single base substitution G A exon_variant ORCA-IN 16 711137 711137 single base substitution G A missense_variant E1160K 3478G>A ORCA-IN 16 711137 711137 single base substitution G A upstream_gene_variant ORCA-IN 16 716374 716374 single base substitution G T downstream_gene_variant ORCA-IN 16 716374 716374 single base substitution G T intron_variant ORCA-IN 16 716374 716374 single base substitution G T upstream_gene_variant ORCA-IN 16 720512 720512 single base substitution C T downstream_gene_variant ORCA-IN 16 721108 721108 single base substitution C T downstream_gene_variant OV-AU 16 696579 696579 single base substitution A C upstream_gene_variant OV-AU 16 702362 702362 single base substitution T C exon_variant OV-AU 16 702362 702362 single base substitution T C intron_variant OV-AU 16 702362 702362 single base substitution T C upstream_gene_variant OV-AU 16 712170 712170 single base substitution G C downstream_gene_variant OV-AU 16 712170 712170 single base substitution G C intron_variant OV-AU 16 712170 712170 single base substitution G C upstream_gene_variant OV-AU 16 716334 716334 single base substitution G T 3_prime_UTR_variant OV-AU 16 716334 716334 single base substitution G T downstream_gene_variant OV-AU 16 716334 716334 single base substitution G T exon_variant OV-AU 16 716334 716334 single base substitution G T missense_variant C1575F 4724G>T OV-AU 16 716334 716334 single base substitution G T missense_variant C1577F 4730G>T OV-AU 16 716334 716334 single base substitution G T missense_variant C174F 521G>T OV-AU 16 716334 716334 single base substitution G T upstream_gene_variant OV-AU 16 718179 718179 single base substitution G C downstream_gene_variant OV-US 16 704990 704990 single base substitution C T downstream_gene_variant OV-US 16 704990 704990 single base substitution C T exon_variant OV-US 16 704990 704990 single base substitution C T intron_variant OV-US 16 704990 704990 single base substitution C T upstream_gene_variant PACA-AU 16 695852 695852 single base substitution G A upstream_gene_variant PACA-AU 16 700264 700264 single base substitution T A exon_variant PACA-AU 16 700264 700264 single base substitution T A missense_variant V97D 290T>A PACA-AU 16 700264 700264 single base substitution T A upstream_gene_variant PACA-AU 16 700357 700358 deletion of <=200bp AG - exon_variant PACA-AU 16 700357 700358 deletion of <=200bp AG - frameshift_variant Q128 PACA-AU 16 700357 700358 deletion of <=200bp AG - upstream_gene_variant PACA-AU 16 703364 703364 single base substitution G A exon_variant PACA-AU 16 703364 703364 single base substitution G A synonymous_variant A382A 1146G>A PACA-AU 16 703364 703364 single base substitution G A upstream_gene_variant PACA-AU 16 716768 716768 single base substitution C T 3_prime_UTR_variant PACA-AU 16 716768 716768 single base substitution C T downstream_gene_variant PACA-AU 16 716768 716768 single base substitution C T exon_variant PACA-AU 16 716768 716768 single base substitution C T synonymous_variant I1660I 4980C>T PACA-AU 16 716768 716768 single base substitution C T synonymous_variant I1662I 4986C>T PACA-AU 16 716768 716768 single base substitution C T synonymous_variant I211I 633C>T PACA-AU 16 716768 716768 single base substitution C T synonymous_variant I259I 777C>T PACA-AU 16 716768 716768 single base substitution C T synonymous_variant I66I 198C>T PACA-AU 16 716768 716768 single base substitution C T upstream_gene_variant PACA-AU 16 719139 719139 single base substitution C T downstream_gene_variant PACA-AU 16 720743 720743 single base substitution G A downstream_gene_variant PACA-AU 16 720896 720896 single base substitution C T downstream_gene_variant PACA-AU 16 721634 721634 single base substitution G T downstream_gene_variant PACA-CA 16 695974 695974 single base substitution G A upstream_gene_variant PACA-CA 16 697338 697338 single base substitution G C upstream_gene_variant PACA-CA 16 700855 700855 single base substitution C A intron_variant PACA-CA 16 700855 700855 single base substitution C A upstream_gene_variant PACA-CA 16 701664 701664 single base substitution C A exon_variant PACA-CA 16 701664 701664 single base substitution C A missense_variant Q253K 757C>A PACA-CA 16 701664 701664 single base substitution C A upstream_gene_variant PACA-CA 16 702652 702652 insertion of <=200bp - C intron_variant PACA-CA 16 702652 702652 insertion of <=200bp - C upstream_gene_variant PACA-CA 16 707456 707456 single base substitution C G downstream_gene_variant PACA-CA 16 707456 707456 single base substitution C G intron_variant PACA-CA 16 707456 707456 single base substitution C G upstream_gene_variant PACA-CA 16 711919 711919 insertion of <=200bp - G 3_prime_UTR_variant PACA-CA 16 711919 711919 insertion of <=200bp - G downstream_gene_variant PACA-CA 16 711919 711919 insertion of <=200bp - G exon_variant PACA-CA 16 711919 711919 insertion of <=200bp - G frameshift_variant V1298G? PACA-CA 16 711919 711919 insertion of <=200bp - G upstream_gene_variant PACA-CA 16 712996 712996 single base substitution G A downstream_gene_variant PACA-CA 16 712996 712996 single base substitution G A exon_variant PACA-CA 16 712996 712996 single base substitution G A intron_variant PACA-CA 16 712996 712996 single base substitution G A upstream_gene_variant PACA-CA 16 713507 713507 single base substitution A G downstream_gene_variant PACA-CA 16 713507 713507 single base substitution A G exon_variant PACA-CA 16 713507 713507 single base substitution A G intron_variant PACA-CA 16 713507 713507 single base substitution A G upstream_gene_variant PACA-CA 16 714829 714829 single base substitution G A downstream_gene_variant PACA-CA 16 714829 714829 single base substitution G A intron_variant PACA-CA 16 714829 714829 single base substitution G A upstream_gene_variant PACA-CA 16 715190 715190 single base substitution C T 5_prime_UTR_variant PACA-CA 16 715190 715190 single base substitution C T downstream_gene_variant PACA-CA 16 715190 715190 single base substitution C T exon_variant PACA-CA 16 715190 715190 single base substitution C T intron_variant PACA-CA 16 715190 715190 single base substitution C T upstream_gene_variant PACA-CA 16 719737 719737 single base substitution C T downstream_gene_variant PACA-CA 16 719854 719854 deletion of <=200bp G - downstream_gene_variant PACA-CA 16 720684 720684 single base substitution G A downstream_gene_variant PACA-CA 16 721102 721102 single base substitution G A downstream_gene_variant PACA-CA 16 721286 721286 single base substitution G A downstream_gene_variant PAEN-AU 16 722398 722398 single base substitution A T downstream_gene_variant PBCA-DE 16 702689 702689 single base substitution G A intron_variant PBCA-DE 16 702689 702689 single base substitution G A upstream_gene_variant PBCA-DE 16 703464 703464 single base substitution C T exon_variant PBCA-DE 16 703464 703464 single base substitution C T intron_variant PBCA-DE 16 703464 703464 single base substitution C T upstream_gene_variant PBCA-DE 16 705597 705597 single base substitution C T downstream_gene_variant PBCA-DE 16 705597 705597 single base substitution C T exon_variant PBCA-DE 16 705597 705597 single base substitution C T synonymous_variant H581H 1743C>T PBCA-DE 16 705597 705597 single base substitution C T upstream_gene_variant PBCA-DE 16 706133 706133 single base substitution G A downstream_gene_variant PBCA-DE 16 706133 706133 single base substitution G A exon_variant PBCA-DE 16 706133 706133 single base substitution G A intron_variant PBCA-DE 16 706133 706133 single base substitution G A upstream_gene_variant PBCA-DE 16 716656 716656 single base substitution A C downstream_gene_variant PBCA-DE 16 716656 716656 single base substitution A C exon_variant PBCA-DE 16 716656 716656 single base substitution A C intron_variant PBCA-DE 16 716656 716656 single base substitution A C upstream_gene_variant PBCA-DE 16 717616 717616 insertion of <=200bp - CATCA 3_prime_UTR_variant PBCA-DE 16 717616 717616 insertion of <=200bp - CATCA downstream_gene_variant PBCA-DE 16 717616 717616 insertion of <=200bp - CATCA exon_variant PBCA-DE 16 717616 717616 insertion of <=200bp - CATCA frameshift_variant A61AS? PBCA-DE 16 717893 717893 single base substitution C G downstream_gene_variant PBCA-DE 16 718749 718749 single base substitution A T downstream_gene_variant PRAD-CA 16 703389 703389 single base substitution G A exon_variant PRAD-CA 16 703389 703389 single base substitution G A missense_variant V391I 1171G>A PRAD-CA 16 703389 703389 single base substitution G A upstream_gene_variant PRAD-CA 16 706449 706449 single base substitution C A downstream_gene_variant PRAD-CA 16 706449 706449 single base substitution C A exon_variant PRAD-CA 16 706449 706449 single base substitution C A missense_variant A705D 2114C>A PRAD-CA 16 706449 706449 single base substitution C A upstream_gene_variant PRAD-UK 16 705801 705801 single base substitution C G downstream_gene_variant PRAD-UK 16 705801 705801 single base substitution C G exon_variant PRAD-UK 16 705801 705801 single base substitution C G missense_variant S626R 1878C>G PRAD-UK 16 705801 705801 single base substitution C G upstream_gene_variant PRAD-UK 16 719411 719411 single base substitution G A downstream_gene_variant PRAD-US 16 703785 703785 single base substitution G A downstream_gene_variant PRAD-US 16 703785 703785 single base substitution G A exon_variant PRAD-US 16 703785 703785 single base substitution G A synonymous_variant K473K 1419G>A PRAD-US 16 703785 703785 single base substitution G A upstream_gene_variant READ-US 16 705360 705360 single base substitution T C downstream_gene_variant READ-US 16 705360 705360 single base substitution T C exon_variant READ-US 16 705360 705360 single base substitution T C missense_variant V537A 1610T>C READ-US 16 705360 705360 single base substitution T C upstream_gene_variant READ-US 16 706435 706435 single base substitution C T downstream_gene_variant READ-US 16 706435 706435 single base substitution C T exon_variant READ-US 16 706435 706435 single base substitution C T synonymous_variant T700T 2100C>T READ-US 16 706435 706435 single base substitution C T upstream_gene_variant READ-US 16 711898 711898 single base substitution G A 3_prime_UTR_variant READ-US 16 711898 711898 single base substitution G A downstream_gene_variant READ-US 16 711898 711898 single base substitution G A exon_variant READ-US 16 711898 711898 single base substitution G A missense_variant R1291Q 3872G>A READ-US 16 711898 711898 single base substitution G A upstream_gene_variant RECA-EU 16 696568 696568 single base substitution A T upstream_gene_variant RECA-EU 16 697340 697340 single base substitution G A upstream_gene_variant RECA-EU 16 713744 713744 single base substitution G T downstream_gene_variant RECA-EU 16 713744 713744 single base substitution G T intron_variant RECA-EU 16 713744 713744 single base substitution G T upstream_gene_variant RECA-EU 16 721227 721227 single base substitution C T downstream_gene_variant SKCA-BR 16 699021 699021 single base substitution T G upstream_gene_variant SKCA-BR 16 703024 703024 single base substitution T C intron_variant SKCA-BR 16 703024 703024 single base substitution T C upstream_gene_variant SKCA-BR 16 704095 704095 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 16 704095 704095 insertion of <=200bp - AT exon_variant SKCA-BR 16 704095 704095 insertion of <=200bp - AT intron_variant SKCA-BR 16 704095 704095 insertion of <=200bp - AT upstream_gene_variant SKCA-BR 16 704278 704278 single base substitution A C downstream_gene_variant SKCA-BR 16 704278 704278 single base substitution A C exon_variant SKCA-BR 16 704278 704278 single base substitution A C intron_variant SKCA-BR 16 704278 704278 single base substitution A C upstream_gene_variant SKCA-BR 16 704302 704302 single base substitution G A downstream_gene_variant SKCA-BR 16 704302 704302 single base substitution G A exon_variant SKCA-BR 16 704302 704302 single base substitution G A intron_variant SKCA-BR 16 704302 704302 single base substitution G A upstream_gene_variant SKCA-BR 16 705300 705300 single base substitution C T downstream_gene_variant SKCA-BR 16 705300 705300 single base substitution C T exon_variant SKCA-BR 16 705300 705300 single base substitution C T splice_region_variant SKCA-BR 16 705300 705300 single base substitution C T upstream_gene_variant SKCA-BR 16 705806 705806 single base substitution C T downstream_gene_variant SKCA-BR 16 705806 705806 single base substitution C T exon_variant SKCA-BR 16 705806 705806 single base substitution C T missense_variant S628F 1883C>T SKCA-BR 16 705806 705806 single base substitution C T upstream_gene_variant SKCA-BR 16 705951 705951 single base substitution A G downstream_gene_variant SKCA-BR 16 705951 705951 single base substitution A G exon_variant SKCA-BR 16 705951 705951 single base substitution A G intron_variant SKCA-BR 16 705951 705951 single base substitution A G upstream_gene_variant SKCA-BR 16 706594 706594 single base substitution T G downstream_gene_variant SKCA-BR 16 706594 706594 single base substitution T G intron_variant SKCA-BR 16 706594 706594 single base substitution T G upstream_gene_variant SKCA-BR 16 708553 708553 single base substitution C T downstream_gene_variant SKCA-BR 16 708553 708553 single base substitution C T exon_variant SKCA-BR 16 708553 708553 single base substitution C T missense_variant P932L 2795C>T SKCA-BR 16 708553 708553 single base substitution C T upstream_gene_variant SKCA-BR 16 708858 708858 single base substitution C T downstream_gene_variant SKCA-BR 16 708858 708858 single base substitution C T intron_variant SKCA-BR 16 708858 708858 single base substitution C T upstream_gene_variant SKCA-BR 16 711614 711614 single base substitution A C 3_prime_UTR_variant SKCA-BR 16 711614 711614 single base substitution A C downstream_gene_variant SKCA-BR 16 711614 711614 single base substitution A C exon_variant SKCA-BR 16 711614 711614 single base substitution A C missense_variant T1231P 3691A>C SKCA-BR 16 711614 711614 single base substitution A C upstream_gene_variant SKCA-BR 16 713789 713789 single base substitution G A downstream_gene_variant SKCA-BR 16 713789 713789 single base substitution G A intron_variant SKCA-BR 16 713789 713789 single base substitution G A upstream_gene_variant SKCA-BR 16 714176 714189 deletion of <=200bp AAACCCCGTGCGTG - downstream_gene_variant SKCA-BR 16 714176 714189 deletion of <=200bp AAACCCCGTGCGTG - intron_variant SKCA-BR 16 714176 714189 deletion of <=200bp AAACCCCGTGCGTG - upstream_gene_variant SKCA-BR 16 714190 714190 single base substitution C G downstream_gene_variant SKCA-BR 16 714190 714190 single base substitution C G intron_variant SKCA-BR 16 714190 714190 single base substitution C G upstream_gene_variant SKCA-BR 16 714224 714224 single base substitution T C downstream_gene_variant SKCA-BR 16 714224 714224 single base substitution T C intron_variant SKCA-BR 16 714224 714224 single base substitution T C upstream_gene_variant SKCA-BR 16 715214 715264 deletion of <=200bp ACCTCAGTCTGCAGCCTGCTAGGGACGCACGGCCACACTCCTGTCTTTCAG - 5_prime_UTR_variant SKCA-BR 16 715214 715264 deletion of <=200bp ACCTCAGTCTGCAGCCTGCTAGGGACGCACGGCCACACTCCTGTCTTTCAG - downstream_gene_variant SKCA-BR 16 715214 715264 deletion of <=200bp ACCTCAGTCTGCAGCCTGCTAGGGACGCACGGCCACACTCCTGTCTTTCAG - exon_variant SKCA-BR 16 715214 715264 deletion of <=200bp ACCTCAGTCTGCAGCCTGCTAGGGACGCACGGCCACACTCCTGTCTTTCAG - intron_variant SKCA-BR 16 715214 715264 deletion of <=200bp ACCTCAGTCTGCAGCCTGCTAGGGACGCACGGCCACACTCCTGTCTTTCAG - upstream_gene_variant SKCA-BR 16 715673 715673 single base substitution C T downstream_gene_variant SKCA-BR 16 715673 715673 single base substitution C T exon_variant SKCA-BR 16 715673 715673 single base substitution C T missense_variant P35S 103C>T SKCA-BR 16 715673 715673 single base substitution C T splice_region_variant SKCA-BR 16 715673 715673 single base substitution C T upstream_gene_variant SKCA-BR 16 715847 715847 single base substitution A G downstream_gene_variant SKCA-BR 16 715847 715847 single base substitution A G intron_variant SKCA-BR 16 715847 715847 single base substitution A G upstream_gene_variant SKCA-BR 16 715992 715992 single base substitution C T 3_prime_UTR_variant SKCA-BR 16 715992 715992 single base substitution C T downstream_gene_variant SKCA-BR 16 715992 715992 single base substitution C T exon_variant SKCA-BR 16 715992 715992 single base substitution C T missense_variant P1493S 4477C>T SKCA-BR 16 715992 715992 single base substitution C T missense_variant P1495S 4483C>T SKCA-BR 16 715992 715992 single base substitution C T missense_variant P92S 274C>T SKCA-BR 16 715992 715992 single base substitution C T upstream_gene_variant SKCA-BR 16 716087 716087 single base substitution C T 3_prime_UTR_variant SKCA-BR 16 716087 716087 single base substitution C T downstream_gene_variant SKCA-BR 16 716087 716087 single base substitution C T exon_variant SKCA-BR 16 716087 716087 single base substitution C T synonymous_variant H123H 369C>T SKCA-BR 16 716087 716087 single base substitution C T synonymous_variant H1524H 4572C>T SKCA-BR 16 716087 716087 single base substitution C T synonymous_variant H1526H 4578C>T SKCA-BR 16 716087 716087 single base substitution C T upstream_gene_variant SKCA-BR 16 718033 718033 single base substitution C T downstream_gene_variant SKCA-BR 16 718288 718288 single base substitution A G downstream_gene_variant SKCA-BR 16 718292 718292 single base substitution T G downstream_gene_variant SKCA-BR 16 720986 720986 single base substitution G A downstream_gene_variant SKCA-BR 16 721406 721406 single base substitution C G downstream_gene_variant SKCM-US 16 700084 700084 single base substitution G A exon_variant SKCM-US 16 700084 700084 single base substitution G A missense_variant G66R 196G>A SKCM-US 16 700084 700084 single base substitution G A upstream_gene_variant SKCM-US 16 700291 700291 single base substitution T G exon_variant SKCM-US 16 700291 700291 single base substitution T G missense_variant F106C 317T>G SKCM-US 16 700291 700291 single base substitution T G upstream_gene_variant SKCM-US 16 701848 701848 single base substitution C T exon_variant SKCM-US 16 701848 701848 single base substitution C T missense_variant P288S 862C>T SKCM-US 16 701848 701848 single base substitution C T upstream_gene_variant SKCM-US 16 703431 703431 single base substitution T C exon_variant SKCM-US 16 703431 703431 single base substitution T C missense_variant F405L 1213T>C SKCM-US 16 703431 703431 single base substitution T C upstream_gene_variant SKCM-US 16 705079 705079 single base substitution C T downstream_gene_variant SKCM-US 16 705079 705079 single base substitution C T exon_variant SKCM-US 16 705079 705079 single base substitution C T synonymous_variant V496V 1488C>T SKCM-US 16 705079 705079 single base substitution C T upstream_gene_variant SKCM-US 16 705369 705369 single base substitution C T downstream_gene_variant SKCM-US 16 705369 705369 single base substitution C T exon_variant SKCM-US 16 705369 705369 single base substitution C T missense_variant S540F 1619C>T SKCM-US 16 705369 705369 single base substitution C T upstream_gene_variant SKCM-US 16 705456 705456 single base substitution C T downstream_gene_variant SKCM-US 16 705456 705456 single base substitution C T exon_variant SKCM-US 16 705456 705456 single base substitution C T missense_variant S569L 1706C>T SKCM-US 16 705456 705456 single base substitution C T upstream_gene_variant SKCM-US 16 706315 706315 single base substitution C G downstream_gene_variant SKCM-US 16 706315 706315 single base substitution C G exon_variant SKCM-US 16 706315 706315 single base substitution C G synonymous_variant P660P 1980C>G SKCM-US 16 706315 706315 single base substitution C G upstream_gene_variant SKCM-US 16 706315 706315 single base substitution C T downstream_gene_variant SKCM-US 16 706315 706315 single base substitution C T exon_variant SKCM-US 16 706315 706315 single base substitution C T synonymous_variant P660P 1980C>T SKCM-US 16 706315 706315 single base substitution C T upstream_gene_variant SKCM-US 16 706349 706349 single base substitution C T downstream_gene_variant SKCM-US 16 706349 706349 single base substitution C T exon_variant SKCM-US 16 706349 706349 single base substitution C T missense_variant R672C 2014C>T SKCM-US 16 706349 706349 single base substitution C T upstream_gene_variant SKCM-US 16 708548 708548 single base substitution C T downstream_gene_variant SKCM-US 16 708548 708548 single base substitution C T exon_variant SKCM-US 16 708548 708548 single base substitution C T synonymous_variant P930P 2790C>T SKCM-US 16 708548 708548 single base substitution C T upstream_gene_variant SKCM-US 16 708645 708645 single base substitution G A downstream_gene_variant SKCM-US 16 708645 708645 single base substitution G A exon_variant SKCM-US 16 708645 708645 single base substitution G A intron_variant SKCM-US 16 708645 708645 single base substitution G A missense_variant G963S 2887G>A SKCM-US 16 708645 708645 single base substitution G A upstream_gene_variant SKCM-US 16 711461 711461 single base substitution C T 3_prime_UTR_variant SKCM-US 16 711461 711461 single base substitution C T downstream_gene_variant SKCM-US 16 711461 711461 single base substitution C T exon_variant SKCM-US 16 711461 711461 single base substitution C T synonymous_variant A1211A 3633C>T SKCM-US 16 711461 711461 single base substitution C T upstream_gene_variant SKCM-US 16 716594 716594 single base substitution C T 3_prime_UTR_variant SKCM-US 16 716594 716594 single base substitution C T downstream_gene_variant SKCM-US 16 716594 716594 single base substitution C T exon_variant SKCM-US 16 716594 716594 single base substitution C T intron_variant SKCM-US 16 716594 716594 single base substitution C T missense_variant T1627M 4880C>T SKCM-US 16 716594 716594 single base substitution C T missense_variant T1629M 4886C>T SKCM-US 16 716594 716594 single base substitution C T missense_variant T226M 677C>T SKCM-US 16 716594 716594 single base substitution C T missense_variant T33M 98C>T SKCM-US 16 716594 716594 single base substitution C T upstream_gene_variant SKCM-US 16 716717 716717 single base substitution G A 3_prime_UTR_variant SKCM-US 16 716717 716717 single base substitution G A downstream_gene_variant SKCM-US 16 716717 716717 single base substitution G A exon_variant SKCM-US 16 716717 716717 single base substitution G A stop_gained W1643* 4929G>A SKCM-US 16 716717 716717 single base substitution G A stop_gained W1645* 4935G>A SKCM-US 16 716717 716717 single base substitution G A stop_gained W194* 582G>A SKCM-US 16 716717 716717 single base substitution G A stop_gained W242* 726G>A SKCM-US 16 716717 716717 single base substitution G A stop_gained W49* 147G>A SKCM-US 16 716717 716717 single base substitution G A upstream_gene_variant SKCM-US 16 717536 717536 single base substitution C T 3_prime_UTR_variant SKCM-US 16 717536 717536 single base substitution C T downstream_gene_variant SKCM-US 16 717536 717536 single base substitution C T exon_variant SKCM-US 16 717536 717536 single base substitution C T missense_variant L1732F 5194C>T SKCM-US 16 717536 717536 single base substitution C T missense_variant L1734F 5200C>T SKCM-US 16 717536 717536 single base substitution C T missense_variant L283F 847C>T SKCM-US 16 717536 717536 single base substitution C T missense_variant L331F 991C>T SKCM-US 16 717536 717536 single base substitution C T synonymous_variant C34C 102C>T SKCM-US 16 720261 720261 single base substitution C T downstream_gene_variant SKCM-US 16 720770 720770 single base substitution C T downstream_gene_variant SKCM-US 16 720896 720896 single base substitution C T downstream_gene_variant SKCM-US 16 720927 720927 single base substitution C T downstream_gene_variant SKCM-US 16 720985 720985 single base substitution C T downstream_gene_variant STAD-US 16 700148 700148 single base substitution A G exon_variant STAD-US 16 700148 700148 single base substitution A G missense_variant H87R 260A>G STAD-US 16 700148 700148 single base substitution A G upstream_gene_variant STAD-US 16 700674 700674 single base substitution G T exon_variant STAD-US 16 700674 700674 single base substitution G T missense_variant R175M 524G>T STAD-US 16 700674 700674 single base substitution G T upstream_gene_variant STAD-US 16 701657 701657 single base substitution G A exon_variant STAD-US 16 701657 701657 single base substitution G A synonymous_variant P250P 750G>A STAD-US 16 701657 701657 single base substitution G A upstream_gene_variant STAD-US 16 701681 701681 single base substitution G T exon_variant STAD-US 16 701681 701681 single base substitution G T synonymous_variant P258P 774G>T STAD-US 16 701681 701681 single base substitution G T upstream_gene_variant STAD-US 16 701703 701703 single base substitution C T exon_variant STAD-US 16 701703 701703 single base substitution C T missense_variant R266W 796C>T STAD-US 16 701703 701703 single base substitution C T upstream_gene_variant STAD-US 16 701719 701719 single base substitution C A exon_variant STAD-US 16 701719 701719 single base substitution C A missense_variant P271Q 812C>A STAD-US 16 701719 701719 single base substitution C A upstream_gene_variant STAD-US 16 702537 702537 single base substitution T C splice_donor_variant STAD-US 16 702537 702537 single base substitution T C upstream_gene_variant STAD-US 16 703790 703790 single base substitution A G downstream_gene_variant STAD-US 16 703790 703790 single base substitution A G exon_variant STAD-US 16 703790 703790 single base substitution A G missense_variant H475R 1424A>G STAD-US 16 703790 703790 single base substitution A G upstream_gene_variant STAD-US 16 705073 705073 single base substitution G A downstream_gene_variant STAD-US 16 705073 705073 single base substitution G A exon_variant STAD-US 16 705073 705073 single base substitution G A synonymous_variant E494E 1482G>A STAD-US 16 705073 705073 single base substitution G A upstream_gene_variant STAD-US 16 708547 708547 single base substitution C G downstream_gene_variant STAD-US 16 708547 708547 single base substitution C G exon_variant STAD-US 16 708547 708547 single base substitution C G missense_variant P930R 2789C>G STAD-US 16 708547 708547 single base substitution C G upstream_gene_variant STAD-US 16 708580 708580 single base substitution G A downstream_gene_variant STAD-US 16 708580 708580 single base substitution G A exon_variant STAD-US 16 708580 708580 single base substitution G A missense_variant R941H 2822G>A STAD-US 16 708580 708580 single base substitution G A upstream_gene_variant STAD-US 16 708999 708999 single base substitution C A downstream_gene_variant STAD-US 16 708999 708999 single base substitution C A exon_variant STAD-US 16 708999 708999 single base substitution C A missense_variant A1000D 2999C>A STAD-US 16 708999 708999 single base substitution C A upstream_gene_variant STAD-US 16 709106 709106 insertion of <=200bp - C downstream_gene_variant STAD-US 16 709106 709106 insertion of <=200bp - C exon_variant STAD-US 16 709106 709106 insertion of <=200bp - C frameshift_variant A1011A? STAD-US 16 709106 709106 insertion of <=200bp - C upstream_gene_variant STAD-US 16 711480 711480 single base substitution G T 3_prime_UTR_variant STAD-US 16 711480 711480 single base substitution G T downstream_gene_variant STAD-US 16 711480 711480 single base substitution G T exon_variant STAD-US 16 711480 711480 single base substitution G T missense_variant D1218Y 3652G>T STAD-US 16 711480 711480 single base substitution G T upstream_gene_variant STAD-US 16 711649 711649 single base substitution C T 3_prime_UTR_variant STAD-US 16 711649 711649 single base substitution C T downstream_gene_variant STAD-US 16 711649 711649 single base substitution C T exon_variant STAD-US 16 711649 711649 single base substitution C T synonymous_variant L1242L 3726C>T STAD-US 16 711649 711649 single base substitution C T upstream_gene_variant STAD-US 16 712018 712018 single base substitution G A 3_prime_UTR_variant STAD-US 16 712018 712018 single base substitution G A downstream_gene_variant STAD-US 16 712018 712018 single base substitution G A exon_variant STAD-US 16 712018 712018 single base substitution G A missense_variant G1331D 3992G>A STAD-US 16 712018 712018 single base substitution G A upstream_gene_variant STAD-US 16 715686 715686 single base substitution A G 3_prime_UTR_variant STAD-US 16 715686 715686 single base substitution A G downstream_gene_variant STAD-US 16 715686 715686 single base substitution A G exon_variant STAD-US 16 715686 715686 single base substitution A G missense_variant E1440G 4319A>G STAD-US 16 715686 715686 single base substitution A G missense_variant E1442G 4325A>G STAD-US 16 715686 715686 single base substitution A G missense_variant E39G 116A>G STAD-US 16 715686 715686 single base substitution A G upstream_gene_variant STAD-US 16 715973 715973 deletion of <=200bp C - 3_prime_UTR_variant STAD-US 16 715973 715973 deletion of <=200bp C - downstream_gene_variant STAD-US 16 715973 715973 deletion of <=200bp C - exon_variant STAD-US 16 715973 715973 deletion of <=200bp C - frameshift_variant S1486 STAD-US 16 715973 715973 deletion of <=200bp C - frameshift_variant S1488 STAD-US 16 715973 715973 deletion of <=200bp C - frameshift_variant S85 STAD-US 16 715973 715973 deletion of <=200bp C - upstream_gene_variant STAD-US 16 716300 716300 single base substitution A G 3_prime_UTR_variant STAD-US 16 716300 716300 single base substitution A G downstream_gene_variant STAD-US 16 716300 716300 single base substitution A G exon_variant STAD-US 16 716300 716300 single base substitution A G missense_variant S1564G 4690A>G STAD-US 16 716300 716300 single base substitution A G missense_variant S1566G 4696A>G STAD-US 16 716300 716300 single base substitution A G missense_variant S163G 487A>G STAD-US 16 716300 716300 single base substitution A G upstream_gene_variant STAD-US 16 716352 716352 single base substitution T C downstream_gene_variant STAD-US 16 716352 716352 single base substitution T C exon_variant STAD-US 16 716352 716352 single base substitution T C splice_donor_variant STAD-US 16 716352 716352 single base substitution T C upstream_gene_variant STAD-US 16 716929 716929 deletion of <=200bp T - 3_prime_UTR_variant STAD-US 16 716929 716929 deletion of <=200bp T - downstream_gene_variant STAD-US 16 716929 716929 deletion of <=200bp T - exon_variant STAD-US 16 716929 716929 deletion of <=200bp T - frameshift_variant F1677 STAD-US 16 716929 716929 deletion of <=200bp T - frameshift_variant F1679 STAD-US 16 716929 716929 deletion of <=200bp T - frameshift_variant F228 STAD-US 16 716929 716929 deletion of <=200bp T - frameshift_variant F276 STAD-US 16 716929 716929 deletion of <=200bp T - frameshift_variant F7 STAD-US 16 716929 716929 deletion of <=200bp T - intron_variant STAD-US 16 720267 720267 single base substitution G A downstream_gene_variant STAD-US 16 720697 720697 single base substitution C T downstream_gene_variant STAD-US 16 720944 720944 single base substitution C T downstream_gene_variant STAD-US 16 721704 721704 single base substitution G A downstream_gene_variant STAD-US 16 721707 721707 deletion of <=200bp C - downstream_gene_variant STAD-US 16 721922 721922 single base substitution G A downstream_gene_variant THCA-SA 16 705873 705873 single base substitution G A downstream_gene_variant THCA-SA 16 705873 705873 single base substitution G A exon_variant THCA-SA 16 705873 705873 single base substitution G A synonymous_variant S650S 1950G>A THCA-SA 16 705873 705873 single base substitution G A upstream_gene_variant THCA-US 16 720708 720708 single base substitution A G downstream_gene_variant UCEC-US 16 698181 698181 single base substitution C T upstream_gene_variant UCEC-US 16 700706 700706 single base substitution C T exon_variant UCEC-US 16 700706 700706 single base substitution C T missense_variant P186S 556C>T UCEC-US 16 700706 700706 single base substitution C T upstream_gene_variant UCEC-US 16 701235 701235 single base substitution G A exon_variant UCEC-US 16 701235 701235 single base substitution G A synonymous_variant P235P 705G>A UCEC-US 16 701235 701235 single base substitution G A upstream_gene_variant UCEC-US 16 701967 701967 single base substitution G T exon_variant UCEC-US 16 701967 701967 single base substitution G T synonymous_variant T327T 981G>T UCEC-US 16 701967 701967 single base substitution G T upstream_gene_variant UCEC-US 16 703523 703523 single base substitution A G downstream_gene_variant UCEC-US 16 703523 703523 single base substitution A G splice_acceptor_variant UCEC-US 16 703523 703523 single base substitution A G upstream_gene_variant UCEC-US 16 703745 703745 single base substitution G A downstream_gene_variant UCEC-US 16 703745 703745 single base substitution G A splice_acceptor_variant UCEC-US 16 703745 703745 single base substitution G A upstream_gene_variant UCEC-US 16 705608 705608 single base substitution T C downstream_gene_variant UCEC-US 16 705608 705608 single base substitution T C exon_variant UCEC-US 16 705608 705608 single base substitution T C missense_variant I585T 1754T>C UCEC-US 16 705608 705608 single base substitution T C upstream_gene_variant UCEC-US 16 706010 706010 insertion of <=200bp - A downstream_gene_variant UCEC-US 16 706010 706010 insertion of <=200bp - A exon_variant UCEC-US 16 706010 706010 insertion of <=200bp - A intron_variant UCEC-US 16 706010 706010 insertion of <=200bp - A upstream_gene_variant UCEC-US 16 706824 706824 single base substitution C T downstream_gene_variant UCEC-US 16 706824 706824 single base substitution C T exon_variant UCEC-US 16 706824 706824 single base substitution C T synonymous_variant A765A 2295C>T UCEC-US 16 706824 706824 single base substitution C T upstream_gene_variant UCEC-US 16 708904 708904 single base substitution C T downstream_gene_variant UCEC-US 16 708904 708904 single base substitution C T exon_variant UCEC-US 16 708904 708904 single base substitution C T synonymous_variant I968I 2904C>T UCEC-US 16 708904 708904 single base substitution C T upstream_gene_variant UCEC-US 16 709252 709252 deletion of <=200bp C - downstream_gene_variant UCEC-US 16 709252 709252 deletion of <=200bp C - exon_variant UCEC-US 16 709252 709252 deletion of <=200bp C - frameshift_variant G1020 UCEC-US 16 709252 709252 deletion of <=200bp C - frameshift_variant G2 UCEC-US 16 709252 709252 deletion of <=200bp C - upstream_gene_variant UCEC-US 16 711941 711941 single base substitution G A 3_prime_UTR_variant UCEC-US 16 711941 711941 single base substitution G A downstream_gene_variant UCEC-US 16 711941 711941 single base substitution G A exon_variant UCEC-US 16 711941 711941 single base substitution G A synonymous_variant S1305S 3915G>A UCEC-US 16 711941 711941 single base substitution G A upstream_gene_variant UCEC-US 16 716291 716291 single base substitution C T 3_prime_UTR_variant UCEC-US 16 716291 716291 single base substitution C T downstream_gene_variant UCEC-US 16 716291 716291 single base substitution C T exon_variant UCEC-US 16 716291 716291 single base substitution C T missense_variant R1561C 4681C>T UCEC-US 16 716291 716291 single base substitution C T missense_variant R1563C 4687C>T UCEC-US 16 716291 716291 single base substitution C T missense_variant R160C 478C>T UCEC-US 16 716291 716291 single base substitution C T upstream_gene_variant UCEC-US 16 716974 716974 single base substitution G A 3_prime_UTR_variant UCEC-US 16 716974 716974 single base substitution G A downstream_gene_variant UCEC-US 16 716974 716974 single base substitution G A exon_variant UCEC-US 16 716974 716974 single base substitution G A intron_variant UCEC-US 16 716974 716974 single base substitution G A missense_variant A1692T 5074G>A UCEC-US 16 716974 716974 single base substitution G A missense_variant A1694T 5080G>A UCEC-US 16 716974 716974 single base substitution G A missense_variant A22T 64G>A UCEC-US 16 716974 716974 single base substitution G A missense_variant A243T 727G>A UCEC-US 16 716974 716974 single base substitution G A missense_variant A291T 871G>A UCEC-US 16 717435 717435 single base substitution G A 3_prime_UTR_variant UCEC-US 16 717435 717435 single base substitution G A downstream_gene_variant UCEC-US 16 717435 717435 single base substitution G A exon_variant UCEC-US 16 717435 717435 single base substitution G A intron_variant UCEC-US 16 717435 717435 single base substitution G A missense_variant A76T 226G>A UCEC-US 16 717435 717435 single base substitution G A missense_variant C1698Y 5093G>A UCEC-US 16 717435 717435 single base substitution G A missense_variant C1700Y 5099G>A UCEC-US 16 717435 717435 single base substitution G A missense_variant C249Y 746G>A UCEC-US 16 717435 717435 single base substitution G A missense_variant C297Y 890G>A UCEC-US 16 720488 720488 single base substitution G T downstream_gene_variant UCEC-US 16 720752 720752 single base substitution C T downstream_gene_variant UCEC-US 16 721776 721776 single base substitution G A downstream_gene_variant UCEC-US 16 722303 722303 single base substitution C T downstream_gene_variant UCEC-US 16 722747 722747 single base substitution C T downstream_gene_variant UCEC-US 16 722748 722748 single base substitution G A downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PT50 COSM5937701 c.416C>T p.A139V Substitution - Missense 16:650566-650566 + TCGA-AA-3713-01 COSM3755036 c.4475G>A p.R1492H Substitution - Missense 16:665990-665990 + TCGA-A3-3320-01 COSM1135821 c.466C>G p.L156V Substitution - Missense 16:650616-650616 + ESCC_BICR_018T COSM5429060 c.3175G>C p.G1059R Substitution - Missense 16:659367-659367 + 587284 COSM1232707 c.425C>T p.T142I Substitution - Missense 16:650575-650575 + TCGA-D5-6927-01 COSM1735146 c.3032delC p.P1013fs*98 Deletion - Frameshift 16:659106-659106 + TCGA-EK-A3GK-01 COSM4853752 c.1847C>T p.S616L Substitution - Missense 16:655701-655701 + CHC197T COSM435723 c.5181G>T p.P1727P Substitution - coding silent 16:667523-667523 + 18 COSM1735146 c.3032delC p.P1013fs*98 Deletion - Frameshift 16:659106-659106 + WSU-HN13 COSM472041 c.2927C>A p.A976D Substitution - Missense 16:658927-658927 + TCGA-D7-6528-01 COSM4062366 c.1482G>A p.E494E Substitution - coding silent 16:655073-655073 + TCGA-BR-4361-01 COSM4062333 c.1424A>G p.H475R Substitution - Missense 16:653790-653790 + CSCC-47-T COSM4540464 c.2847G>A p.R949R Substitution - coding silent 16:658605-658605 + BCM759T COSM4956718 c.1447G>A p.A483T Substitution - Missense 16:655038-655038 + RMS88_ COSM4988950 c.2299C>T p.R767C Substitution - Missense 16:656828-656828 + TCGA-EE-A2GR-06 COSM3511328 c.317T>G p.F106C Substitution - Missense 16:650291-650291 + TCGA-G4-6302-01 COSM435663 c.1610T>C p.V537A Substitution - Missense 16:655360-655360 + TCGA-39-5027-01 COSM704233 c.4771C>G p.L1591V Substitution - Missense 16:666485-666485 + TCGA-EI-6917-01 COSM3421142 c.3872G>A p.R1291Q Substitution - Missense 16:661898-661898 + S00941 COSM5663678 c.3628delC p.L1210fs*94 Deletion - Frameshift 16:661456-661456 + ESCC_BICR_058T COSM5430550 c.1094T>A p.I365N Substitution - Missense 16:652507-652507 + RW7213 COSM4649918 c.4247C>T p.T1416M Substitution - Missense 16:662780-662780 + TCGA-EE-A29V-06 COSM3511434 c.2790C>T p.P930P Substitution - coding silent 16:658548-658548 + TCGA-G4-6588-01 COSM1378788 c.4227C>T p.V1409V Substitution - coding silent 16:662760-662760 + TCGA-BC-A3KF-01 COSM4927808 c.70T>C p.S24P Substitution - Missense 16:649822-649822 + TCGA-AC-A23H-01 COSM3818476 c.4318G>A p.E1440K Substitution - Missense 16:665685-665685 + PTC-10C COSM4129321 c.4663T>C p.C1555R Substitution - Missense 16:666273-666273 + TCGA-AM-5821-01 COSM435709 c.3879A>G p.P1293P Substitution - coding silent 16:661905-661905 + ESO-0255 COSM1270443 c.4253G>T p.W1418L Substitution - Missense 16:662786-662786 + TCGA-AZ-6601-01 COSM5142331 c.2806C>T p.L936F Substitution - Missense 16:658564-658564 + 8049042 COSM3387561 c.290T>A p.V97D Substitution - Missense 16:650264-650264 + MAVER-1 COSM1740260 c.652C>T p.R218C Substitution - Missense 16:651087-651087 + SNUH_G73_S1 COSM3755024 c.2697C>A p.H899Q Substitution - Missense 16:658275-658275 + ESOSCC152T COSM1172343 c.4713C>G p.I1571M Substitution - Missense 16:666323-666323 + EGC8 COSM3275950 c.4506C>T p.Y1502Y Substitution - coding silent 16:666021-666021 + CPCG0269-F1 COSM4880334 c.1171G>A p.V391I Substitution - Missense 16:653389-653389 + TCGA-D5-6540-01 COSM1735146 c.3032delC p.P1013fs*98 Deletion - Frameshift 16:659106-659106 + BCM439T COSM4951882 c.2529G>A p.R843R Substitution - coding silent 16:657817-657817 + TCGA-EA-A3HR-01 COSM4843303 c.5110G>A p.D1704N Substitution - Missense 16:667452-667452 + TCGA-AM-5821-01 COSM435663 c.1610T>C p.V537A Substitution - Missense 16:655360-655360 + TCGA-CK-4951-01 COSM5148652 c.3180C>T p.G1060G Substitution - coding silent 16:659372-659372 + B96 COSM1749683 c.2677G>C p.G893R Substitution - Missense 16:658255-658255 + BN28T COSM1609587 c.1904G>A p.G635D Substitution - Missense 16:655827-655827 + C008 COSM5524189 c.4177G>A p.D1393N Substitution - Missense 16:662710-662710 + TCGA-G4-6302-01 COSM3691147 c.3716C>A p.T1239N Substitution - Missense 16:661639-661639 + ACINAR01 COSM1735146 c.3032delC p.P1013fs*98 Deletion - Frameshift 16:659106-659106 + TCGA-NH-A5IV-01 COSM5182652 c.1887G>A p.P629P Substitution - coding silent 16:655810-655810 + SNUH_G10_S1 COSM3755024 c.2697C>A p.H899Q Substitution - Missense 16:658275-658275 + 1_PRE-TREATMENT COSM1720988 c.5056C>T p.P1686S Substitution - Missense 16:666956-666956 + 6115250 COSM5554608 c.414A>G p.G138G Substitution - coding silent 16:650564-650564 + S00933 COSM316557 c.375G>A p.R125R Substitution - coding silent 16:650349-650349 + SNU-C2B COSM3275915 c.4332C>T p.S1444S Substitution - coding silent 16:665699-665699 + TCGA-CK-5913-01 COSM5154008 c.1509T>C p.T503T Substitution - coding silent 16:655100-655100 + 1N31-VS-1T31 COSM3272863 c.1208G>A p.R403H Substitution - Missense 16:653426-653426 + TCGA-22-5472-01 COSM704333 c.1286C>A p.A429E Substitution - Missense 16:653577-653577 + TCGA-BR-7707-01 COSM4062305 c.1122+2T>C p.? Unknown 16:652537-652537 + HCT15 COSM1678735 c.605C>T p.P202L Substitution - Missense 16:651040-651040 + TCGA-IZ-A6M9-01 COSM3988638 c.2473+2T>G p.? Unknown 16:657223-657223 + CSCC-27-T COSM4485512 c.2941C>T p.P981S Substitution - Missense 16:658941-658941 + CSCC-27-T COSM4485450 c.2934C>T p.A978A Substitution - coding silent 16:658934-658934 + TCGA-EE-A29M-06 COSM3511404 c.2014C>T p.R672C Substitution - Missense 16:656349-656349 + TCGA-G3-A25U-01 COSM4649918 c.4247C>T p.T1416M Substitution - Missense 16:662780-662780 + KM12 COSM1678736 c.3916C>T p.L1306F Substitution - Missense 16:661942-661942 + SC_9022 COSM5500367 c.3313G>A p.G1105S Substitution - Missense 16:660636-660636 + TCGA-CG-5721-01 COSM4062298 c.750G>A p.P250P Substitution - coding silent 16:651657-651657 + BD114T COSM5504148 c.5081G>A p.G1694D Substitution - Missense 16:666981-666981 + TCGA-BR-6566-01 COSM4062478 c.3726C>T p.L1242L Substitution - coding silent 16:661649-661649 + TCGA-CM-6674-01 COSM1378759 c.2752C>T p.R918C Substitution - Missense 16:658330-658330 + 1_RESISTANT COSM1720988 c.5056C>T p.P1686S Substitution - Missense 16:666956-666956 + PTC-70C COSM3755032 c.3789C>T p.G1263G Substitution - coding silent 16:661712-661712 + T3145 COSM4460685 c.1176C>T p.I392I Substitution - coding silent 16:653394-653394 + HCA7 COSM3275375 c.3567C>T p.R1189R Substitution - coding silent 16:661395-661395 + TCGA-18-3410-01 COSM704261 c.3915G>C p.S1305S Substitution - coding silent 16:661941-661941 + PDA_004 COSM4129321 c.4663T>C p.C1555R Substitution - Missense 16:666273-666273 + TCGA-EJ-7783-01 COSM1470933 c.1419G>A p.K473K Substitution - coding silent 16:653785-653785 + B63 COSM1749689 c.4888C>A p.Q1630K Substitution - Missense 16:666676-666676 + 8016470 COSM3387563 c.1146G>A p.A382A Substitution - coding silent 16:653364-653364 + TCGA-DK-A3IN-01 COSM3795099 c.4680C>T p.F1560F Substitution - coding silent 16:666290-666290 + TCGA-AM-5821-01 COSM435723 c.5181G>T p.P1727P Substitution - coding silent 16:667523-667523 + TCGA-CK-4951-01 COSM5148651 c.1612C>T p.L538L Substitution - coding silent 16:655362-655362 + H2009 COSM1193699 c.308C>G p.S103C Substitution - Missense 16:650282-650282 + 134398 COSM324307 c.439G>A p.D147N Substitution - Missense 16:650589-650589 + BD124T COSM5493352 c.4851C>T p.D1617D Substitution - coding silent 16:666565-666565 + DLD1 COSM3275782 c.4224C>T p.G1408G Substitution - coding silent 16:662757-662757 + 523T COSM3272858 c.1153G>A p.V385M Substitution - Missense 16:653371-653371 + LIM2551 COSM4644017 c.3300G>C p.P1100P Substitution - coding silent 16:660623-660623 + CAL27 COSM472041 c.2927C>A p.A976D Substitution - Missense 16:658927-658927 + H23 COSM1196308 c.2839G>A p.A947T Substitution - Missense 16:658597-658597 + S01366 COSM316559 c.2977G>T p.V993F Substitution - Missense 16:658977-658977 + CSCC-5-T COSM4505868 c.703C>T p.P235S Substitution - Missense 16:651233-651233 + 587338 COSM1232704 c.5126C>T p.T1709I Substitution - Missense 16:667468-667468 + Gp5D COSM3276065 c.5039T>C p.M1680T Substitution - Missense 16:666939-666939 + TCGA-AA-3506-01 COSM5098373 c.3990C>T p.A1330A Substitution - coding silent 16:662016-662016 + CT-TC COSM4989647 c.1770G>A p.M590I Substitution - Missense 16:655624-655624 + TCGA-DW-7841-01 COSM1678739 c.4681C>A p.R1561S Substitution - Missense 16:666291-666291 + TCGA-06-0158 COSM2150135 c.1277C>T p.S426L Substitution - Missense 16:653568-653568 + TCGA-AZ-6598-01 COSM3272863 c.1208G>A p.R403H Substitution - Missense 16:653426-653426 + TCGA-BT-A0S7-01 COSM417297 c.1308G>A p.R436R Substitution - coding silent 16:653599-653599 + TCGA-AP-A059-01 COSM973358 c.5093G>A p.C1698Y Substitution - Missense 16:667435-667435 + TCGA-ER-A19D-06 COSM3511402 c.1980C>G p.P660P Substitution - coding silent 16:656315-656315 + PT50 COSM5937702 c.4148C>T p.S1383F Substitution - Missense 16:662681-662681 + 587332 COSM1232705 c.154G>A p.A52T Substitution - Missense 16:650042-650042 + H2073 COSM1197416 c.4829G>A p.R1610Q Substitution - Missense 16:666543-666543 + 420 COSM4432051 c.5057C>T p.P1686L Substitution - Missense 16:666957-666957 + CHC2052T COSM4789889 c.3814A>C p.T1272P Substitution - Missense 16:661737-661737 + TCGA-FW-A3R5-06 COSM3888831 c.1488C>T p.V496V Substitution - coding silent 16:655079-655079 + PT08_1 COSM5893893 c.1234-5C>T p.? Unknown 16:653520-653520 + HX11T COSM1609578 c.979A>T p.T327S Substitution - Missense 16:651965-651965 + LUAD-S01405 COSM398951 c.3298C>T p.P1100S Substitution - Missense 16:660621-660621 + TCGA-CD-A4MJ-01 COSM4062302 c.812C>A p.P271Q Substitution - Missense 16:651719-651719 + 587220 COSM1232702 c.1090G>A p.V364I Substitution - Missense 16:652503-652503 + TCGA-EE-A2A6-06 COSM3511859 c.4880C>T p.T1627M Substitution - Missense 16:666594-666594 + YUKAT COSM4502809 c.622C>T p.P208S Substitution - Missense 16:651057-651057 + D-12 COSM4766827 c.3694C>T p.L1232F Substitution - Missense 16:661617-661617 + TCGA-EA-A410-01 COSM4828606 c.2502G>A p.A834A Substitution - coding silent 16:657790-657790 + DLD1 COSM4623403 c.217T>C p.Y73H Substitution - Missense 16:650105-650105 + FM474T COSM673843 c.599C>A p.P200H Substitution - Missense 16:651034-651034 + SNUH_G10_S1 COSM435652 c.749C>T p.P250L Substitution - Missense 16:651656-651656 + TCGA-DA-A1I5-06 COSM3511403 c.1980C>T p.P660P Substitution - coding silent 16:656315-656315 + YUKAT COSM5385307 c.3591C>T p.L1197L Substitution - coding silent 16:661419-661419 + pfg181T COSM1735146 c.3032delC p.P1013fs*98 Deletion - Frameshift 16:659106-659106 + TCGA-B5-A11Y-01 COSM973315 c.4681C>T p.R1561C Substitution - Missense 16:666291-666291 + CHEWS007 COSM973054 c.2235G>A p.P745P Substitution - coding silent 16:656764-656764 + TCGA-AP-A059-01 COSM973350 c.5074G>A p.A1692T Substitution - Missense 16:666974-666974 + CPCG0158-F1 COSM4966280 c.2114C>A p.A705D Substitution - Missense 16:656449-656449 + Pat_15_B COSM1735146 c.3032delC p.P1013fs*98 Deletion - Frameshift 16:659106-659106 + 587222 COSM1232703 c.2005G>A p.D669N Substitution - Missense 16:656340-656340 + MO_1012 COSM5564103 c.3217C>T p.R1073C Substitution - Missense 16:660090-660090 + TCGA-06-0157-01 COSM3402445 c.1000G>A p.V334M Substitution - Missense 16:651986-651986 + PTC-14C COSM4129325 c.4709C>A p.P1570Q Substitution - Missense 16:666319-666319 + CSCC-49-T COSM4495338 c.4518C>T p.S1506S Substitution - coding silent 16:666033-666033 + SC_9090 COSM5548848 c.5187C>T p.A1729A Substitution - coding silent 16:667529-667529 + TCGA-BR-8683-01 COSM4062471 c.3652G>T p.D1218Y Substitution - Missense 16:661480-661480 + H23 COSM1196482 c.824C>T p.T275M Substitution - Missense 16:651731-651731 + LUAD-RT-S01818 COSM383873 c.722C>G p.S241C Substitution - Missense 16:651252-651252 + TCGA-A5-A0VP-01 COSM973096 c.2904C>T p.I968I Substitution - coding silent 16:658904-658904 + PTC-515C COSM4129317 c.4179C>T p.D1393D Substitution - coding silent 16:662712-662712 + S00944 COSM316558 c.3901G>T p.G1301* Substitution - Nonsense 16:661927-661927 + TCGA-34-5240-01 COSM704260 c.4004T>C p.L1335S Substitution - Missense 16:662030-662030 + AOCS-155-3-5 COSM4141889 c.4724G>T p.C1575F Substitution - Missense 16:666334-666334 + CHC1704T COSM4803853 c.4248G>T p.T1416T Substitution - coding silent 16:662781-662781 + CSCC-47-T COSM4494694 c.4388C>T p.A1463V Substitution - Missense 16:665755-665755 + S00035 COSM5656713 c.2390G>T p.R797L Substitution - Missense 16:657138-657138 + TCGA-33-4566-01 COSM704315 c.1960G>A p.E654K Substitution - Missense 16:655883-655883 + ESCC_168 COSM5648723 c.2612G>A p.R871Q Substitution - Missense 16:658190-658190 + TCGA-04-1342-01 COSM133448 c.1364_1365TT>CC p.V455A Substitution - Missense 16:653655-653656 + SH-0622 COSM5018401 c.3072delG p.E1025fs*86 Deletion - Frameshift 16:659264-659264 + CCK81 COSM4620706 c.4134C>T p.G1378G Substitution - coding silent 16:662320-662320 + MOLT-4 COSM1678739 c.4681C>A p.R1561S Substitution - Missense 16:666291-666291 + 46M COSM5589359 c.1199G>A p.G400E Substitution - Missense 16:653417-653417 + PTC-28C COSM4129272 c.1872C>T p.S624S Substitution - coding silent 16:655795-655795 + TCGA-AP-A0LM-01 COSM972964 c.556C>T p.P186S Substitution - Missense 16:650706-650706 + KM12 COSM4638962 c.4083G>A p.G1361G Substitution - coding silent 16:662269-662269 + TCGA-AC-A23H-01 COSM3818432 c.3172G>A p.E1058K Substitution - Missense 16:659364-659364 + TARGET-20-PARBIU-04A-01D COSM5487416 c.1285G>T p.A429S Substitution - Missense 16:653576-653576 + P-Thy041 COSM3988638 c.2473+2T>G p.? Unknown 16:657223-657223 + Pat_15_B COSM3511859 c.4880C>T p.T1627M Substitution - Missense 16:666594-666594 + TCGA-B4-5836-01 COSM1493756 c.527A>G p.N176S Substitution - Missense 16:650677-650677 + TCGA-BR-4184-01 COSM4062549 c.4740+2T>C p.? Unknown 16:666352-666352 + CSCC-42-T COSM4536052 c.2262G>A p.R754R Substitution - coding silent 16:656791-656791 + BD49T COSM5498186 c.876G>A p.P292P Substitution - coding silent 16:651862-651862 + CPCG0103-P2 COSM3396244 c.4546G>T p.A1516S Substitution - Missense 16:666061-666061 + S01366 COSM316559 c.2977G>T p.V993F Substitution - Missense 16:658977-658977 + 0124_CRUK_PC_0124_T1_DNA COSM5420980 c.1878C>G p.S626R Substitution - Missense 16:655801-655801 + TCGA-AA-3712-01 COSM3755022 c.2199G>A p.Q733Q Substitution - coding silent 16:656534-656534 + TCGA-GV-A3JX-01 COSM1302197 c.114G>A p.L38L Substitution - coding silent 16:650002-650002 + MO_1184 COSM5567392 c.4146-1G>T p.? Unknown 16:662678-662678 + TCGA-D5-6922-01 COSM1378757 c.2005G>T p.D669Y Substitution - Missense 16:656340-656340 + TCGA-G4-6322-01 COSM3691140 c.2748G>A p.S916S Substitution - coding silent 16:658326-658326 + CSCC-7-T COSM3273795 c.3027C>T p.P1009P Substitution - coding silent 16:659101-659101 + TCGA-WS-AB45-01 COSM5189985 c.1787G>A p.R596H Substitution - Missense 16:655641-655641 + TCGA-G4-6321-01 COSM3755036 c.4475G>A p.R1492H Substitution - Missense 16:665990-665990 + TCGA-CK-5913-01 COSM1378768 c.3306C>T p.P1102P Substitution - coding silent 16:660629-660629 + ESCC_BICR_031T COSM5441056 c.3827G>T p.W1276L Substitution - Missense 16:661750-661750 + PD13767a COSM5786925 c.3080C>T p.A1027V Substitution - Missense 16:659272-659272 + S00933 COSM316557 c.375G>A p.R125R Substitution - coding silent 16:650349-650349 + TCGA-A2-A0T5-01 COSM3818400 c.861A>C p.A287A Substitution - coding silent 16:651847-651847 + TCGA-HF-7132-01 COSM4062411 c.2822G>A p.R941H Substitution - Missense 16:658580-658580 + TCGA-06-6701-01 COSM3748004 c.1333T>G p.C445G Substitution - Missense 16:653624-653624 + OSCC-GB_00560111 COSM4883778 c.2883C>A p.S961R Substitution - Missense 16:658641-658641 + TCGA-E2-A155-01 COSM435672 c.2769G>A p.L923L Substitution - coding silent 16:658527-658527 + TCGA-D1-A17U-01 COSM972996 c.1234-2A>G p.? Unknown 16:653523-653523 + LC_C6 COSM1189127 c.1289G>T p.R430M Substitution - Missense 16:653580-653580 + BD225T COSM5508701 c.1966G>A p.E656K Substitution - Missense 16:655889-655889 + TCGA-AZ-4615-01 COSM435663 c.1610T>C p.V537A Substitution - Missense 16:655360-655360 + TCGA-A6-3808-01 COSM291366 c.1169C>A p.A390E Substitution - Missense 16:653387-653387 + CSCC-27-T COSM4477557 c.2163C>T p.D721D Substitution - coding silent 16:656498-656498 + TCGA-CK-4951-01 COSM5148653 c.3787G>A p.G1263S Substitution - Missense 16:661710-661710 + S00938 COSM5663311 c.3146G>T p.R1049L Substitution - Missense 16:659338-659338 + T3503 COSM1378782 c.3924C>T p.Y1308Y Substitution - coding silent 16:661950-661950 + T3202 COSM4741119 c.3517C>A p.L1173M Substitution - Missense 16:661345-661345 + I2L-P7-Tumor-Organoid COSM5363253 c.4458delC p.P1488fs*11 Deletion - Frameshift 16:665973-665973 + S02322 COSM5691263 c.2400C>T p.F800F Substitution - coding silent 16:657148-657148 + SW48 COSM4261862 c.3669A>G p.T1223T Substitution - coding silent 16:661497-661497 + HCA7 COSM4612064 c.3031_3032insC p.A1014fs*193 Insertion - Frameshift 16:659105-659106 + CHEWS007 COSM2150135 c.1277C>T p.S426L Substitution - Missense 16:653568-653568 + PT08_2 COSM5893893 c.1234-5C>T p.? Unknown 16:653520-653520 + TCGA-G4-6628-01 COSM1378760 c.3056C>T p.P1019L Substitution - Missense 16:659248-659248 + pfg008T COSM4748347 c.1535T>C p.V512A Substitution - Missense 16:655126-655126 + CSCC-31-T COSM4480883 c.2463C>T p.L821L Substitution - coding silent 16:657211-657211 + TCGA-D1-A177-01 COSM972980 c.981G>T p.T327T Substitution - coding silent 16:651967-651967 + ESCC_110 COSM5639193 c.756A>G p.P252P Substitution - coding silent 16:651663-651663 + Pat_41_B COSM5851339 c.182G>A p.S61N Substitution - Missense 16:650070-650070 + ASHPC_0008_Pa_P COSM3787207 c.757C>A p.Q253K Substitution - Missense 16:651664-651664 + BD114T COSM5504146 c.4333C>A p.P1445T Substitution - Missense 16:665700-665700 + BZ09 COSM5500367 c.3313G>A p.G1105S Substitution - Missense 16:660636-660636 + BD180T COSM5495176 c.1950G>T p.S650S Substitution - coding silent 16:655873-655873 + CSCC-6-T COSM4481808 c.2547C>T p.A849A Substitution - coding silent 16:657835-657835 + T368 COSM4741122 c.4956delC p.G1654fs*6 Deletion - Frameshift 16:666744-666744 + TCGA-FW-A3R5-06 COSM3888842 c.2887G>A p.G963S Substitution - Missense 16:658645-658645 + KM12 COSM1678736 c.3916C>T p.L1306F Substitution - Missense 16:661942-661942 + TCGA-AA-3713-01 COSM3755022 c.2199G>A p.Q733Q Substitution - coding silent 16:656534-656534 + PD14441a COSM5767797 c.4458C>G p.S1486R Substitution - Missense 16:665973-665973 + PTC-7C COSM4129273 c.1921T>C p.L641L Substitution - coding silent 16:655844-655844 + B96-Tumor COSM1749683 c.2677G>C p.G893R Substitution - Missense 16:658255-658255 + sysucc-1370T COSM5470557 c.988G>A p.A330T Substitution - Missense 16:651974-651974 + TCGA-BR-8361-01 COSM4062410 c.2789C>G p.P930R Substitution - Missense 16:658547-658547 + Pat_59_A COSM5851417 c.4877C>T p.T1626I Substitution - Missense 16:666591-666591 + ME043T COSM228633 c.1820C>T p.P607L Substitution - Missense 16:655674-655674 + TCGA-AM-5821-01 COSM435652 c.749C>T p.P250L Substitution - Missense 16:651656-651656 + TCGA-AA-3815-01 COSM1378755 c.1356A>G p.P452P Substitution - coding silent 16:653647-653647 + CHC2052T COSM4789889 c.3814A>C p.T1272P Substitution - Missense 16:661737-661737 + Pat_41_B COSM5851374 c.2906G>A p.G969D Substitution - Missense 16:658906-658906 + T2944 COSM4741120 c.4541G>A p.R1514H Substitution - Missense 16:666056-666056 + CSCC-38-T COSM4564764 c.1429_1430GG>AA p.G477K Substitution - Missense 16:653795-653796 + TCGA-CK-4951-01 COSM1735146 c.3032delC p.P1013fs*98 Deletion - Frameshift 16:659106-659106 + LS411 COSM3273292 c.2034C>T p.S678S Substitution - coding silent 16:656369-656369 + PD11327a COSM5800034 c.4603A>T p.T1535S Substitution - Missense 16:666118-666118 + CSCC-44-T COSM4489668 c.3510C>T p.A1170A Substitution - coding silent 16:661169-661169 + CPCG0103-P1 COSM3396244 c.4546G>T p.A1516S Substitution - Missense 16:666061-666061 + WSU-HN12 COSM4601250 c.1752G>T p.E584D Substitution - Missense 16:655606-655606 + SC_9047 COSM5562973 c.2490G>A p.P830P Substitution - coding silent 16:657778-657778 + TCGA-CK-4951-01 COSM5148649 c.433C>T p.Q145* Substitution - Nonsense 16:650583-650583 + T407 COSM4741117 c.1101T>C p.F367F Substitution - coding silent 16:652514-652514 + PTC-70C COSM435709 c.3879A>G p.P1293P Substitution - coding silent 16:661905-661905 + TCGA-DM-A28K-01 COSM1378829 c.4544C>T p.T1515M Substitution - Missense 16:666059-666059 + T407 COSM4741116 c.523A>G p.R175G Substitution - Missense 16:650673-650673 + BD95T COSM5505614 c.232C>T p.P78S Substitution - Missense 16:650120-650120 + COLO205 COSM4621305 c.5211C>G p.R1737R Substitution - coding silent 16:667553-667553 + B63-Tumor COSM1749689 c.4888C>A p.Q1630K Substitution - Missense 16:666676-666676 + CSCC-27-T COSM4505868 c.703C>T p.P235S Substitution - Missense 16:651233-651233 + BCM439T COSM4951882 c.2529G>A p.R843R Substitution - coding silent 16:657817-657817 + SCC-9 COSM472041 c.2927C>A p.A976D Substitution - Missense 16:658927-658927 + TCGA-UB-A7MD-01 COSM4932994 c.3154G>A p.V1052I Substitution - Missense 16:659346-659346 + TCGA-D7-6518-01 COSM3272720 c.796C>T p.R266W Substitution - Missense 16:651703-651703 + PD7210a COSM5769028 c.3983C>T p.T1328M Substitution - Missense 16:662009-662009 + S02322 COSM5691262 c.2397C>T p.L799L Substitution - coding silent 16:657145-657145 + CSCC-31-T COSM4460685 c.1176C>T p.I392I Substitution - coding silent 16:653394-653394 + I2L-P7-Tumor-Organoid COSM5363634 c.1247C>T p.A416V Substitution - Missense 16:653538-653538 + TCGA-A6-6653-01 COSM5092101 c.559+5G>T p.? Unknown 16:650714-650714 + BD178T COSM5500367 c.3313G>A p.G1105S Substitution - Missense 16:660636-660636 + S02322 COSM5691264 c.2463C>G p.L821L Substitution - coding silent 16:657211-657211 + BD231T COSM973315 c.4681C>T p.R1561C Substitution - Missense 16:666291-666291 + TCGA-A6-3809-01 COSM5086815 c.3096C>T p.S1032S Substitution - coding silent 16:659288-659288 + TCGA-AM-5821-01 COSM3755036 c.4475G>A p.R1492H Substitution - Missense 16:665990-665990 + CSCC-31-T COSM4464175 c.1320C>T p.F440F Substitution - coding silent 16:653611-653611 + 2012_Recurrent COSM5346069 c.2124G>A p.M708I Substitution - Missense 16:656459-656459 + CN-AML-NR-08-Dx COSM435652 c.749C>T p.P250L Substitution - Missense 16:651656-651656 + TCGA-06-2559-01 COSM3402457 c.4378C>T p.R1460W Substitution - Missense 16:665745-665745 + YUGATOR COSM5385328 c.5042_5043CC>TT p.S1681F Substitution - Missense 16:666942-666943 + SNU-C2B COSM4651274 c.1647C>T p.H549H Substitution - coding silent 16:655397-655397 + TCGA-G2-A2EC-01 COSM1302215 c.2785G>A p.E929K Substitution - Missense 16:658543-658543 + LIM2551 COSM4644010 c.535A>G p.T179A Substitution - Missense 16:650685-650685 + CHC197T COSM435652 c.749C>T p.P250L Substitution - Missense 16:651656-651656 + TCGA-D1-A15Z-01 COSM973032 c.1754T>C p.I585T Substitution - Missense 16:655608-655608 + CHC892T COSM4960055 c.4552G>A p.E1518K Substitution - Missense 16:666067-666067 + PTC-28C COSM3755032 c.3789C>T p.G1263G Substitution - coding silent 16:661712-661712 + TCGA-D1-A103-01 COSM973233 c.3915G>A p.S1305S Substitution - coding silent 16:661941-661941 + DN14065 COSM5962842 c.4351G>A p.A1451T Substitution - Missense 16:665718-665718 + SS6003314 COSM3273238 c.1804C>T p.R602W Substitution - Missense 16:655658-655658 + TCGA-F5-6702-01 COSM435663 c.1610T>C p.V537A Substitution - Missense 16:655360-655360 + TCGA-BR-8487-01 COSM4062294 c.260A>G p.H87R Substitution - Missense 16:650148-650148 + TCGA-HU-A4H8-01 COSM4062485 c.3992G>A p.G1331D Substitution - Missense 16:662018-662018 + HCT-15 COSM1678735 c.605C>T p.P202L Substitution - Missense 16:651040-651040 + P05-3859 COSM248337 c.4756G>T p.V1586L Substitution - Missense 16:666470-666470 + 855_CLM COSM472041 c.2927C>A p.A976D Substitution - Missense 16:658927-658927 + TCGA-AY-6196-01 COSM1378773 c.3526G>T p.A1176S Substitution - Missense 16:661354-661354 + TCGA-DK-A1A5-01 COSM417296 c.1436C>T p.T479M Substitution - Missense 16:653802-653802 + RMS2028 COSM5880476 c.2081T>A p.M694K Substitution - Missense 16:656416-656416 + TCGA-BS-A0UF-01 COSM972967 c.705G>A p.P235P Substitution - coding silent 16:651235-651235 + TCGA-37-4135-01 COSM704306 c.2839G>T p.A947S Substitution - Missense 16:658597-658597 + T3091 COSM4741118 c.2239G>A p.A747T Substitution - Missense 16:656768-656768 + TCGA-F4-6459-01 COSM5171121 c.1663G>A p.D555N Substitution - Missense 16:655413-655413 + TCGA-BG-A18B-01 COSM973054 c.2235G>A p.P745P Substitution - coding silent 16:656764-656764 + S19_post COSM5575082 c.4608delT p.D1536fs*16 Deletion - Frameshift 16:666123-666123 + TCGA-HU-A4H3-01 COSM4062295 c.524G>T p.R175M Substitution - Missense 16:650674-650674 + TCGA-CG-4444-01 COSM4062547 c.4690A>G p.S1564G Substitution - Missense 16:666300-666300 + HCT15 COSM3275782 c.4224C>T p.G1408G Substitution - coding silent 16:662757-662757 + TCGA-AG-3592-01 COSM3421128 c.2100C>T p.T700T Substitution - coding silent 16:656435-656435 + T276 COSM4741124 c.5238C>T p.P1746P Substitution - coding silent 16:667580-667580 + RMS85_ COSM4988950 c.2299C>T p.R767C Substitution - Missense 16:656828-656828 + PTC-10C COSM4129272 c.1872C>T p.S624S Substitution - coding silent 16:655795-655795 + B89-16-Tumor COSM1749691 c.5214C>A p.N1738K Substitution - Missense 16:667556-667556 + TCGA-D8-A1XQ-01 COSM3818469 c.3810G>A p.Q1270Q Substitution - coding silent 16:661733-661733 + CSCC-56-T COSM4502809 c.622C>T p.P208S Substitution - Missense 16:651057-651057 + TCGA-EK-A3GM-01 COSM4823461 c.3524C>G p.S1175C Substitution - Missense 16:661352-661352 + 2250245 COSM5029901 c.1766G>A p.R589H Substitution - Missense 16:655620-655620 + sysucc-1370T COSM3272672 c.663C>T p.H221H Substitution - coding silent 16:651098-651098 + HCA7 COSM4630243 c.3625G>A p.V1209M Substitution - Missense 16:661453-661453 + TCGA-CK-4951-01 COSM5148650 c.1329G>A p.G443G Substitution - coding silent 16:653620-653620 + CHC197T COSM3755025 c.3001C>A p.P1001T Substitution - Missense 16:659001-659001 + DLD1 COSM1678735 c.605C>T p.P202L Substitution - Missense 16:651040-651040 + T22 COSM5342842 c.4818C>T p.S1606S Substitution - coding silent 16:666532-666532 + TCGA-AA-3710-01 COSM5104860 c.3899C>T p.A1300V Substitution - Missense 16:661925-661925 + PD18768a COSM5790585 c.3393C>T p.G1131G Substitution - coding silent 16:661052-661052 + ESCC_103 COSM5638149 c.520G>T p.V174F Substitution - Missense 16:650670-650670 + TCGA-DA-A3F8-06 COSM3511864 c.4929G>A p.W1643* Substitution - Nonsense 16:666717-666717 + PD4975a COSM3275914 c.4312-5C>T p.? Unknown 16:665674-665674 + LIM2551 COSM4644018 c.4023C>T p.D1341D Substitution - coding silent 16:662049-662049 + C058 COSM5525828 c.2068C>T p.R690W Substitution - Missense 16:656403-656403 + TCGA-D9-A3Z1-06 COSM3511349 c.1213T>C p.F405L Substitution - Missense 16:653431-653431 + TCGA-AA-3663-01 COSM3755036 c.4475G>A p.R1492H Substitution - Missense 16:665990-665990 + B83-Tumor COSM3932422 c.4788T>G p.S1596R Substitution - Missense 16:666502-666502 + TCGA-G4-6321-01 COSM3755022 c.2199G>A p.Q733Q Substitution - coding silent 16:656534-656534 + PTC-53C COSM3755036 c.4475G>A p.R1492H Substitution - Missense 16:665990-665990 + SW1222 COSM4654760 c.4228G>A p.V1410M Substitution - Missense 16:662761-662761 + TCGA-AO-A1KR-01 COSM1479054 c.1853C>T p.P618L Substitution - Missense 16:655776-655776 + 587234 COSM1232708 c.2747C>T p.S916L Substitution - Missense 16:658325-658325 + DU-145 COSM1678737 c.4225G>T p.V1409F Substitution - Missense 16:662758-662758 + TCGA-AM-5821-01 COSM3755032 c.3789C>T p.G1263G Substitution - coding silent 16:661712-661712 + Pat_63_B COSM5851415 c.4621C>T p.L1541F Substitution - Missense 16:666231-666231 + COLO201 COSM4621305 c.5211C>G p.R1737R Substitution - coding silent 16:667553-667553 + 718T COSM4381595 c.3853A>G p.I1285V Substitution - Missense 16:661776-661776 + TCGA-A3-3316-01 COSM472041 c.2927C>A p.A976D Substitution - Missense 16:658927-658927 + TCGA-AZ-6598-01 COSM1378758 c.2069G>A p.R690Q Substitution - Missense 16:656404-656404 + 18 COSM5745271 c.2773G>T p.G925C Substitution - Missense 16:658531-658531 + ccRCC-30 COSM1665015 c.2918C>T p.P973L Substitution - Missense 16:658918-658918 + TCGA-AD-6548-01 COSM5129053 c.1685G>A p.R562Q Substitution - Missense 16:655435-655435 + TCGA-P4-A5E6-01 COSM3988639 c.2499C>T p.P833P Substitution - coding silent 16:657787-657787 + DU-145 COSM1678738 c.4634A>C p.K1545T Substitution - Missense 16:666244-666244 + CSCC-17-T COSM4483360 c.2695C>T p.H899Y Substitution - Missense 16:658273-658273 + S00944 COSM316558 c.3901G>T p.G1301* Substitution - Nonsense 16:661927-661927 + ESCC_40 COSM5629335 c.2352A>T p.R784R Substitution - coding silent 16:657100-657100 + 169 COSM3728976 c.2895+8C>T p.? Unknown 16:658661-658661 + PTC-70C COSM435663 c.1610T>C p.V537A Substitution - Missense 16:655360-655360 + B89-16 COSM1749691 c.5214C>A p.N1738K Substitution - Missense 16:667556-667556 + TCGA-AZ-4313-01 COSM973315 c.4681C>T p.R1561C Substitution - Missense 16:666291-666291 + WSU-HN12 COSM472041 c.2927C>A p.A976D Substitution - Missense 16:658927-658927 + BN01T COSM1609585 c.1610T>G p.V537G Substitution - Missense 16:655360-655360 + ESCC_BICR_040T COSM5429910 c.1674C>G p.F558L Substitution - Missense 16:655424-655424 + TCGA-D3-A2JG-06 COSM3511387 c.1619C>T p.S540F Substitution - Missense 16:655369-655369 + ZZUFHECRKL-G020T COSM4129272 c.1872C>T p.S624S Substitution - coding silent 16:655795-655795 + TCGA-AY-6197-01 COSM3755022 c.2199G>A p.Q733Q Substitution - coding silent 16:656534-656534 + TCGA-BR-6452-01 COSM4062301 c.774G>T p.P258P Substitution - coding silent 16:651681-651681 + TCGA-BR-7707-01 COSM4062532 c.4319A>G p.E1440G Substitution - Missense 16:665686-665686 + TCGA-AP-A0LM-01 COSM973056 c.2295C>T p.A765A Substitution - coding silent 16:656824-656824 + CLL115 COSM1290579 c.4666A>G p.T1556A Substitution - Missense 16:666276-666276 + pfg125T COSM4748346 c.447G>C p.Q149H Substitution - Missense 16:650597-650597 + 1_PRE-TREATMENT COSM1720987 c.4312-7C>T p.? Unknown 16:665672-665672 + TCGA-13-1504-01 COSM73290 c.1474G>A p.G492S Substitution - Missense 16:655065-655065 + TCGA-FP-8211-01 COSM4062420 c.2999C>A p.A1000D Substitution - Missense 16:658999-658999 + 387 COSM4427262 c.1505A>G p.H502R Substitution - Missense 16:655096-655096 + SMS-CTR COSM4989647 c.1770G>A p.M590I Substitution - Missense 16:655624-655624 + LUAD-B00523 COSM331820 c.848G>T p.R283L Substitution - Missense 16:651834-651834 + CHEWS019 COSM4579213 c.198G>A p.G66G Substitution - coding silent 16:650086-650086 + CHC1704T COSM4803853 c.4248G>T p.T1416T Substitution - coding silent 16:662781-662781 + TCGA-AA-A02O-01 COSM300927 c.5016G>A p.K1672K Substitution - coding silent 16:666916-666916 + T3174 COSM3275945 c.4457_4458insC p.C1489fs*6 Insertion - Frameshift 16:665972-665973 + TCGA-EB-A3XB-01 COSM3511389 c.1706C>T p.S569L Substitution - Missense 16:655456-655456 + PTC-10C COSM4129323 c.4677C>A p.T1559T Substitution - coding silent 16:666287-666287 + RH30SJ_ COSM3273417 c.2714C>T p.S905L Substitution - Missense 16:658292-658292 + TCGA-G4-6586-01 COSM1378756 c.1527C>A p.A509A Substitution - coding silent 16:655118-655118 + BCM759T COSM4956718 c.1447G>A p.A483T Substitution - Missense 16:655038-655038 + CSCC-27-T COSM4516843 c.2380_2381CC>TT p.P794F Substitution - Missense 16:657128-657129 + 587234 COSM1232709 c.4976T>C p.V1659A Substitution - Missense 16:666764-666764 + TCGA-DK-A3IK-01 COSM1302229 c.4807G>T p.V1603F Substitution - Missense 16:666521-666521 + DN120F1 COSM5962659 c.2465G>C p.R822P Substitution - Missense 16:657213-657213 + TCGA-DA-A1IA-06 COSM3511906 c.5194C>T p.L1732F Substitution - Missense 16:667536-667536 + ESCC_44 COSM5630019 c.4930G>T p.D1644Y Substitution - Missense 16:666718-666718 + 226 COSM4425836 c.5046G>A p.L1682L Substitution - coding silent 16:666946-666946 + Pat_46_A COSM5851408 c.4334C>T p.P1445L Substitution - Missense 16:665701-665701 + CHC892T COSM4960055 c.4552G>A p.E1518K Substitution - Missense 16:666067-666067 + TCGA-AM-5821-01 COSM3755025 c.3001C>A p.P1001T Substitution - Missense 16:659001-659001 + TCGA-AA-3712-01 COSM435663 c.1610T>C p.V537A Substitution - Missense 16:655360-655360 + TCGA-GF-A6C8-06 COSM3888828 c.862C>T p.P288S Substitution - Missense 16:651848-651848 + TCGA-06-0158-01 COSM2150135 c.1277C>T p.S426L Substitution - Missense 16:653568-653568 + MO_1316 COSM5550410 c.2119G>A p.A707T Substitution - Missense 16:656454-656454 + CN-AML-08-T COSM435652 c.749C>T p.P250L Substitution - Missense 16:651656-651656 + 8057574 COSM3387578 c.4980C>T p.I1660I Substitution - coding silent 16:666768-666768 + Pat_41_B COSM1378829 c.4544C>T p.T1515M Substitution - Missense 16:666059-666059 + T2969 COSM4741115 c.387A>T p.R129S Substitution - Missense 16:650361-650361 + CSCC-16-T COSM1196482 c.824C>T p.T275M Substitution - Missense 16:651731-651731 + TCGA-EE-A29E-06 COSM3511703 c.3633C>T p.A1211A Substitution - coding silent 16:661461-661461 + PT49 COSM5936246 c.1557-8C>T p.? Unknown 16:655299-655299 + PT24_1 COSM5904440 c.2033C>T p.S678F Substitution - Missense 16:656368-656368 + TCGA-AZ-4313-01 COSM5138235 c.3991G>A p.G1331S Substitution - Missense 16:662017-662017 + TCGA-CK-4950-01 COSM435723 c.5181G>T p.P1727P Substitution - coding silent 16:667523-667523 + 3N52-VS-3T52 COSM4983427 c.136C>T p.R46W Substitution - Missense 16:650024-650024 + CSCC-18-T COSM4471187 c.1704C>T p.P568P Substitution - coding silent 16:655454-655454 + TCGA-C5-A1BQ-01 COSM4842265 c.1830G>A p.Q610Q Substitution - coding silent 16:655684-655684 + HCT8 COSM3275782 c.4224C>T p.G1408G Substitution - coding silent 16:662757-662757 + TCGA-06-5408-01 COSM3402447 c.1189G>A p.V397M Substitution - Missense 16:653407-653407 + CHC433T COSM3755032 c.3789C>T p.G1263G Substitution - coding silent 16:661712-661712 + 1020 COSM3272792 c.1110C>T p.H370H Substitution - coding silent 16:652523-652523 + DLD1 COSM4623408 c.3052G>T p.G1018C Substitution - Missense 16:659126-659126 + ESO-864 COSM1270444 c.5209C>T p.R1737C Substitution - Missense 16:667551-667551 + TCGA-B5-A11E-01 COSM973001 c.1380-1G>A p.? Unknown 16:653745-653745 + TCGA-A5-A0GW-01 COSM973123 c.3060delC p.A1021fs*90 Deletion - Frameshift 16:659252-659252 + CSCC-37-T COSM3273474 c.2772C>T p.P924P Substitution - coding silent 16:658530-658530 + ZZUFHECRKL-G045T COSM4129272 c.1872C>T p.S624S Substitution - coding silent 16:655795-655795 + 718LT COSM4381595 c.3853A>G p.I1285V Substitution - Missense 16:661776-661776 + SM-4AX83 COSM5953289 c.3383C>T p.P1128L Substitution - Missense 16:660706-660706 + TCGA-37-4133-01 COSM704307 c.2680C>T p.P894S Substitution - Missense 16:658258-658258 + PD5956a COSM5772077 c.2561C>T p.S854F Substitution - Missense 16:657849-657849 + TCGA-EE-A180-06 COSM3511324 c.196G>A p.G66R Substitution - Missense 16:650084-650084 + OSCC-GB_00590111 COSM4888670 c.3478G>A p.E1160K Substitution - Missense 16:661137-661137 + 1_RESISTANT COSM1720987 c.4312-7C>T p.? Unknown 16:665672-665672 + TCGA-G4-6321-01 COSM3755024 c.2697C>A p.H899Q Substitution - Missense 16:658275-658275 + TCGA-AY-6386-01 COSM435663 c.1610T>C p.V537A Substitution - Missense 16:655360-655360 + 587350 COSM1232706 c.1723G>A p.V575M Substitution - Missense 16:655577-655577 + STC291 COSM5055061 c.3028delG p.A1011fs*100 Deletion - Frameshift 16:659102-659102 + TCGA-AZ-4315-01 COSM1378782 c.3924C>T p.Y1308Y Substitution - coding silent 16:661950-661950 + TCGA-AM-5821-01 COSM3755024 c.2697C>A p.H899Q Substitution - Missense 16:658275-658275 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.511903 16p13.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.K952R c.2855A>G 16 708613 LUAD A G Missense p.Q1474R c.4421A>G 16 715788 HNSC A G Missense p.S1564G c.4690A>G 16 716300 STAD A G Missense p.T1556A c.4666A>G 16 716276 CLL A G SpliceAcceptorSNV . c.1234-2A>G 16 703523 UCEC A T Missense p.T1412S c.4234A>T 16 712767 LUAD C A Missense p.A390E c.1169C>A 16 703387 COREAD C A Missense p.A429E c.1286C>A 16 703577 LUSC C A Missense p.H333N c.997C>A 16 701983 LUAD C A Missense p.L1234M c.3700C>A 16 711623 STAD C A Missense p.Q428K c.1282C>A 16 703573 HNSC CC TT Missense p.A1011V c.3032_3033delinsTT 16 709106 CM C - Frameshift p.A1021Qfs*90 c.3060delC 16 709252 UCEC C G Missense p.D1598E c.4794C>G 16 716508 LUAD C G Missense p.L156V c.466C>G 16 700616 RCCC C G Missense p.L1591V c.4771C>G 16 716485 LUSC C G Nonsense p.Y692* c.2076C>G 16 706411 HNSC C G Synonymous p.P660P c.1980C>G 16 706315 CM C T IntronicSNV . c.1557-41C>T 16 705266 CM C T IntronicSNV . c.1557-8C>T 16 705299 CM C T IntronicSNV . c.1967-6C>T 16 706296 CM C T IntronicSNV . c.2203-79C>T 16 706653 PIA C T IntronicSNV . c.4435-69C>T 16 715881 CM C T Missense p.L1732F c.5194C>T 16 717536 CM C T Missense p.P1622S c.4864C>T 16 716578 CM C T Missense p.P256L c.767C>T 16 701674 CM C T Missense p.P542L c.1625C>T 16 705375 CM C T Missense p.P607L c.1820C>T 16 705674 CM C T Missense p.P618L c.1853C>T 16 705776 BRCA C T Missense p.P894S c.2680C>T 16 708258 LUSC C T Missense p.R1460W c.4378C>T 16 715745 GBM C T Missense p.R266W c.796C>T 16 701703 STAD C T Missense p.R672C c.2014C>T 16 706349 CM C T Missense p.S426L c.1277C>T 16 703568 GBM C T Missense p.S540F c.1619C>T 16 705369 CM C T Missense p.T1627M c.4880C>T 16 716594 CM C T Missense p.T479M c.1436C>T 16 703802 BLCA C T Nonsense p.R1291* c.3871C>T 16 711897 GBM C T Synonymous p.F1560F c.4680C>T 16 716290 BLCA C T Synonymous p.F311F c.933C>T 16 701919 CM C T Synonymous p.I1285I c.3855C>T 16 711778 HNSC C T Synonymous p.I968I c.2904C>T 16 708904 UCEC C T Synonymous p.L1591L c.4771C>T 16 716485 HNSC C T Synonymous p.L671L c.2013C>T 16 706348 LUAD C T Synonymous p.P660P c.1980C>T 16 706315 CM C T Synonymous p.P930P c.2790C>T 16 708548 CM G A IntronicSNV . c.1967-169G>A 16 706133 MB G A Missense p.D1340N c.4018G>A 16 712044 HNSC G A Missense p.D147N c.439G>A 16 700589 SCLC G A Missense p.E1440K c.4318G>A 16 715685 HNSC G A Missense p.E929K c.2785G>A 16 708543 BLCA G A Missense p.G492S c.1474G>A 16 705065 OV G A Missense p.G66R c.196G>A 16 700084 CM G A Missense p.V334M c.1000G>A 16 701986 GBM G A Missense p.V394I c.1180G>A 16 703398 STAD G A Missense p.V397M c.1189G>A 16 703407 GBM G A Nonsense p.W1643* c.4929G>A 16 716717 CM G A Synonymous p.E1494E c.4482G>A 16 715997 LUAD G A Synonymous p.E494E c.1482G>A 16 705073 STAD G A Synonymous p.K1672K c.5016G>A 16 716916 COREAD G A Synonymous p.K473K c.1419G>A 16 703785 PRAD G A Synonymous p.L38L c.114G>A 16 700002 BLCA G A Synonymous p.L923L c.2769G>A 16 708527 BRCA G A Synonymous p.R125R c.375G>A 16 700349 SCLC G A Synonymous p.R436R c.1308G>A 16 703599 BLCA G C Missense p.E1580Q c.4738G>C 16 716348 HNSC G C Synonymous p.S1305S c.3915G>C 16 711941 LUSC GG TT SpliceDonorBlockSubstitution . c.5004_5004+1delinsTT 16 716792 LUAD G T IntronicSNV . c.4312-22G>T 16 715657 RCCC G T Missense p.A1569S c.4705G>T 16 716315 LUAD G T Missense p.A947S c.2839G>T 16 708597 LUSC G T Missense p.E123D c.369G>T 16 700343 LUAD G T Missense p.V1603F c.4807G>T 16 716521 BLCA G T Missense p.V993F c.2977G>T 16 708977 SCLC G T Missense p.W1418L c.4253G>T 16 712786 ESCA G T Nonsense p.G1301* c.3901G>T 16 711927 SCLC G T SpliceAcceptorSNV . c.841-1G>T 16 701826 HNSC G T Synonymous p.T327T c.981G>T 16 701967 UCEC T C Missense p.I585T c.1754T>C 16 705608 UCEC T C Missense p.L1335S c.4004T>C 16 712030 LUSC T C Synonymous p.H819H c.2457T>C 16 707205 LUAD T G Missense p.C445G c.1333T>G 16 703624 GBM T G Missense p.F106C c.317T>G 16 700291 CM TT CC Missense p.V455A c.1364_1365delinsCC 16 703655 OV